Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_assertion description "[The genes involved in the RET-GDNF signaling and/or EDN3-EDNRB signaling pathways have been analyzed as candidates for CCHS; however, only a few patients have mutations of the RET, EDN3, and GDNF genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_assertion evidence source_evidence_literature NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_assertion SIO_000772 14566559 NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_assertion wasDerivedFrom befree-20140225 NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_assertion wasGeneratedBy ECO_0000203 NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658177.RA615MJNYc0Vs2XbxogHQldsG5Pj99E2HGjGGMCtDDETc130_provenance.