Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_assertion description "[Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_assertion evidence source_evidence_literature NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_assertion SIO_000772 25196463 NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_assertion wasDerivedFrom befree-2016 NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_assertion wasGeneratedBy ECO_0000203 NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217760.RA6rSW1uY3zSN8E_6tJpI8CCvByLXzoPkBS3bxC3iu8kE130_provenance.