Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion description "[Although mutations in eight different genes (EDNRB, EDN3, ECE1, SOX10, RET, GDNF, NTN, SIP1) have been identified in affected individuals, it is now clear that RET and EDNRB are the primary genes implicated in the etiology of HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion evidence source_evidence_literature NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion SIO_000772 16618617 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion wasDerivedFrom befree-20140225 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion wasGeneratedBy ECO_0000203 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.