Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_assertion description "[Germline mutations of BRCA2 are predicted to account for approximately 35% of families with multiple case, early onset female breast cancer, and they are also associated with an increased risk of male breast cancer, ovarian cancer, prostate cancer and pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_assertion evidence source_evidence_literature NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_assertion SIO_000772 8988179 NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_assertion wasDerivedFrom befree-2016 NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_assertion wasGeneratedBy ECO_0000203 NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365349.RAoRgtHYtArBBdW5RrVo_ftlEqkwuH7DqcSobU64P9VCI130_provenance.