Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_assertion description "[Rare haplotypes at ATM (P(corr) = 0.044) and BARD1 (P(corr) = 0.012) were associated with ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_assertion evidence source_evidence_literature NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_assertion SIO_000772 19584272 NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_assertion wasDerivedFrom befree-2016 NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_assertion wasGeneratedBy ECO_0000203 NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.
- befree-2016 importedOn "2016-02-19" NP749886.RA2fnO0rJja9EjgM_ezamsi22AnEEozfVdoQYp7OubXms130_provenance.