Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_assertion description "[Women with family histories suggestive of an increased risk of ovarian carcinoma who have not had a deleterious BRCA1 or BRCA2 mutation identified are commonly suggested to consider ovarian carcinoma screening with transvaginal ultrasound and/or assessment of CA 125 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_assertion evidence source_evidence_literature NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_assertion SIO_000772 15948173 NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_assertion wasDerivedFrom befree-20140225 NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_assertion wasGeneratedBy ECO_0000203 NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173747.RAryET50TILoPkijiJGYgO3dNSye1npJVDTZwN_Sl3Thw130_provenance.