Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_assertion description "[Women carrying two copies of the MDM2 SNP309 variant may be at greater risk of endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_assertion evidence source_evidence_literature NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_assertion SIO_000772 18398041 NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_assertion wasDerivedFrom befree-20140225 NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_assertion wasGeneratedBy ECO_0000203 NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811491.RAExjCfXyvDQ-vTnbBCuwZJw1rchpi_BVF5aCYbYK_WRA130_provenance.