Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_assertion description "[SNP c.*1287C>T (rs12516) of the BRCA1 gene may have potential use as a genetic marker of an increased risk of developing breast cancer and likely represents a non-coding sequence variation in BRCA1 that impacts BRCA1 function and leads to increased early-onset and/or familial breast cancer risk in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_assertion evidence source_evidence_literature NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_assertion SIO_000772 25339023 NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_assertion wasDerivedFrom befree-2016 NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_assertion wasGeneratedBy ECO_0000203 NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231846.RAwLFSkhW9Uj18F1yoD8qv-2HGB0ROU3kn7ql25oXUyjQ130_provenance.