Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_assertion description "[As it is well known that the prevalence of gene mutations varies between different populations, we studied the prevalence of PALB2 mutations in a Dutch cohort of non-BRCA1/2 familial PC (FPC) families and in non-BRCA1/2 familial BC (FBC) families with at least one PC case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_assertion evidence source_evidence_literature NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_assertion SIO_000772 22166947 NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_assertion wasDerivedFrom befree-20150227 NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_assertion wasGeneratedBy ECO_0000203 NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP271138.RApLdTb_SM9qG4heu_1iFXSXyS15x96aM29ldNqAZP-b0130_provenance.