Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_assertion description "[We sought somatic mutations in the corresponding genes in the CRCs of the patients harboring the germline lesions and found biallelic inactivation of FANCM, LAMB4, PTCHD3, LAMC3, and TREX2, potentially implicating these genes as tumor suppressors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_assertion evidence source_evidence_literature NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_assertion SIO_000772 23585368 NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_assertion wasDerivedFrom befree-2016 NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_assertion wasGeneratedBy ECO_0000203 NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1069180.RAPBevPVXDU0nXIR5I4HlKhVSMr98VrwutCzHsgXyhpdI130_provenance.