Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_assertion wasGeneratedBy ECO_0000203 NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_assertion wasDerivedFrom befree-20140225 NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_assertion SIO_000772 9731534 NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_assertion evidence source_evidence_literature NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_assertion description "[The gene defect for hereditary papillary renal carcinoma (HPRC) has recently been mapped to chromosome 7q, and germline mutations of MET (also known as c-met) at 7q31 have been detected in patients with HPRC (ref.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP899285.RAlGNuqxyrQzN6I-A6yAdVXNsS-TwKq1lfRRs_lK4V0zQ130_provenance.