Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion evidence source_evidence_literature NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion SIO_000772 20353281 NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion wasDerivedFrom gad-20150221 NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion wasGeneratedBy ECO_0000203 NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.