Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_assertion description "[Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_assertion evidence source_evidence_literature NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_assertion SIO_000772 10458491 NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_assertion wasDerivedFrom befree-2016 NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_assertion wasGeneratedBy ECO_0000203 NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP261072.RA3lnd2gl2rYMnOSMgS2fDRgzspTOpzGATiLs4Twcve9Y130_provenance.