Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_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." NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_assertion evidence source_evidence_literature NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_assertion SIO_000772 16618617 NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_assertion wasDerivedFrom befree-20140225 NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_assertion wasGeneratedBy ECO_0000203 NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869785.RAhj-TjhylIALIhG7rIFPkaDWUJ60J2jPuwnVvC07Cvl8130_provenance.