Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- befree-2016 importedOn "2016-02-19" NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_assertion wasGeneratedBy ECO_0000203 NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_assertion wasDerivedFrom befree-2016 NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_assertion SIO_000772 21246292 NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_assertion evidence source_evidence_literature NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.
- NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_assertion description "[The identification of BRCA1/BRCA2 mutations in women with ovarian cancer allows for accurate predictive genetic testing of their at-risk relatives, who can then avail themselves of early detection and risk reduction strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866242.RAAUyxeLtcS4cpnEPGhn4GH_4-MOzxWuHQb3PzcNo3YgM130_provenance.