Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_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." NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_assertion evidence source_evidence_literature NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_assertion SIO_000772 16618617 NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_assertion wasDerivedFrom befree-2016 NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_assertion wasGeneratedBy ECO_0000203 NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.
- befree-2016 importedOn "2016-02-19" NP545156.RAHiqY3Scd_30rDOhzRhHq5aujxCt30eDmVfBJYNEp_x4130_provenance.