Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_assertion description "[We hypothesized that germline mutations in the p16INK4A, p14ARF or CDK4 genes might contribute to some cases of familial UMM, or to some cases of UMM associated with another melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_assertion evidence source_evidence_literature NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_assertion SIO_000772 10732752 NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_assertion wasDerivedFrom befree-2016 NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_assertion wasGeneratedBy ECO_0000203 NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.
- befree-2016 importedOn "2016-02-19" NP278866.RAY8TGnD4Ym6YCvYpv2rampl_s0rHAHQ2HV38XbVCAxQg130_provenance.