Remove artifacts from refs

components/legacy/index.tsx

@@ -68,9 +68,9 @@ export const GeneTermFromVariantTerm = MetaNode('GeneTermFromVariantTerm')
   })
   .story(props => ({
     abstract: `The closest gene to the variant was found using MyVariant.info\\ref{doi:10.1093/bioinformatics/btac017}.`,
-    introduction: `MyVariant.info is a REST web service for querying and retrieving common variant annotation data [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
-    methods: `${props.inputs?.variant ? props.inputs.variant : 'The variant'} is queried with the MyVariant.info REST web API to resolve up to date annotations [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017} from which the closest gene is extracted from either dbSNP, ClinVar, or SnpEff.`,
-    legend: `The closest gene to ${props.inputs?.variant ? props.inputs.variant : 'the variant'}, as reported by MyVariant.info [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
+    introduction: `MyVariant.info is a REST web service for querying and retrieving common variant annotation data\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
+    methods: `${props.inputs?.variant ? props.inputs.variant : 'The variant'} is queried with the MyVariant.info REST web API to resolve up to date annotations\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017} from which the closest gene is extracted from either dbSNP, ClinVar, or SnpEff.`,
+    legend: `The closest gene to ${props.inputs?.variant ? props.inputs.variant : 'the variant'}, as reported by MyVariant.info\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
   }))
   .build()
 
@@ -117,9 +117,9 @@ export const VariantInfoFromVariantTermMyVarintInfo = MetaNode('VariantInfoFromV
   })
   .story(props => ({
     abstract: `The closest gene to the variant was found using MyVariant.info\\ref{doi:10.1093/bioinformatics/btac017}.`,
-    introduction: `MyVariant.info is a REST web service for querying and retrieving common variant annotation data [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
-    methods: `${props.inputs?.variant ? props.inputs.variant : 'The variant'} is queried with the MyVariant.info REST web API to resolve up to date annotations [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017} from which the closest gene is extracted from either dbSNP, ClinVar, or SnpEff.`,
-    legend: `The closest gene to ${props.inputs?.variant ? props.inputs.variant : 'the variant'}, as reported by MyVariant.info [\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
+    introduction: `MyVariant.info is a REST web service for querying and retrieving common variant annotation data\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
+    methods: `${props.inputs?.variant ? props.inputs.variant : 'The variant'} is queried with the MyVariant.info REST web API to resolve up to date annotations\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017} from which the closest gene is extracted from either dbSNP, ClinVar, or SnpEff.`,
+    legend: `The closest gene to ${props.inputs?.variant ? props.inputs.variant : 'the variant'}, as reported by MyVariant.info\\ref{doi:10.1186/s13059-016-0953-9}\\ref{doi:10.1093/bioinformatics/btac017}.`,
   }))
   .build()
 

components/service/regulatoryElementInfo/service.tsx

@@ -97,8 +97,8 @@ export const GetRegulatoryElementPosition = MetaNode('GetRegulatoryElementPositi
     let response = await getRegulatoryElementsSetPosition(regElemeIdsSet);
     return response;
   }).story(props => ({
-    abstract: `Genomic positions of provided unique regulatory element identifiers were retrieved from CFDE Linked Data Hub [\\ref{CFDE Linked Data Hub, https://ldh.genome.network/cfde/ldh/}].`,
-    introduction: `CFDE LDH is a graph-based network that facilitates access to excerpted regulatory information from external databases and studies including SCREEN, GTEx, and EN-TEx [\\ref{doi:10.1038/s41586-020-2493-4},\\ref{doi:10.1126/science.aaz1776},\\ref{doi:10.1126/science.aar3146}]`,
+    abstract: `Genomic positions of provided unique regulatory element identifiers were retrieved from CFDE Linked Data Hub\\ref{CFDE Linked Data Hub, https://ldh.genome.network/cfde/ldh/}.`,
+    introduction: `CFDE LDH is a graph-based network that facilitates access to excerpted regulatory information from external databases and studies including SCREEN, GTEx, and EN-TEx\\ref{doi:10.1038/s41586-020-2493-4}\\ref{doi:10.1126/science.aaz1776}\\ref{doi:10.1126/science.aar3146}`,
     methods: `Input regulatory element identifiers were queried through CFDE LDH API endpoints and their GRCh38 genomic positions, including chr, start, and end, were retrieved from the JSON response.`,
     legend: `A table displaying the GRCh38 genomic postion of the given regulatory elements`,
   })).build()