Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_assertion description "[Mutation screening and DNA sequencing of the MET gene, which is mapped to 7q31, revealed only the presence of simple sequence polymorphisms but no apparent acquired disease-associated mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_assertion evidence source_evidence_literature NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_assertion SIO_000772 9485032 NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_assertion wasDerivedFrom befree-20140225 NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_assertion wasGeneratedBy ECO_0000203 NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297580.RA67WYv3im_pf6W8r0ZjfKlZOIqzOFWEv2nr59bNPj6tw130_provenance.