Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_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." NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_assertion evidence source_evidence_literature NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_assertion SIO_000772 16618617 NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_assertion wasDerivedFrom befree-20140225 NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_assertion wasGeneratedBy ECO_0000203 NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618718.RAWdqQmERuzuurYNTU-OepBoeE7m3RpKRIxF2wQOLSavo130_provenance.