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- source_evidence_literature type ECO_0000212 NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_assertion description "[Several of these variants are in or near genes with a biological rationale for conferring EOC risk, including ZFP36L1 and RAD51B for mucinous EOC (rs17106154, OR�=�1.17, P�=�0.029, n�=�1,483 cases), GRB10 for endometrioid and clear cell EOC (rs2190503, P�=�0.014, n�=�2,903 cases), and C22orf26/BPIL2 for LMP serous EOC (rs9609538, OR�=�0.86, P�=�0.0043, n�=�892 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_assertion evidence source_evidence_literature NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_assertion SIO_000772 24190013 NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_assertion wasDerivedFrom befree-20150227 NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_assertion wasGeneratedBy ECO_0000203 NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.
- befree-20150227 importedOn "2015-02-27" NP981643.RAYJKshUq96HQ7j6WIXre4XfxxA7v4HswosFau2KZy8Ug130_provenance.