Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_assertion description "[Four single nucleotide polymorphisms (SNPs) in MDM2 and p14(ARF) (MDM2-rs2279744, MDM2-rs937283, p14(ARF)-rs3731217, and p14(ARF)-rs3088440) were genotyped in 156 patients with SGC and 511 cancer-free controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_assertion evidence source_evidence_literature NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_assertion SIO_000772 23145162 NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_assertion wasDerivedFrom befree-20140225 NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_assertion wasGeneratedBy ECO_0000203 NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184502.RAohUlFLy7cVUljd-EnLzEmMMhIM5ygHC6dCiH6yDSAfc130_provenance.