Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_assertion description "[Eleven variants in nine genes (ABL1, CCNB2, CDKN1A, CCND3, E2F2, CDK2, E2F3, CDC2, and CDK7) were associated with risk of ovarian cancer in at least one genetic model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_assertion evidence source_evidence_literature NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_assertion SIO_000772 19738611 NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_assertion wasDerivedFrom gad-20150221 NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_assertion wasGeneratedBy ECO_0000203 NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116247.RABCxgzM6KjQBbvRgL-HT7ct4pG3D1eYcQN6FOgL2CpQg130_provenance.