Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_assertion description "[The insertion/deletion variant in CYP19A1 (cytochrome P450 family 19 subfamily A polypeptide 1) appears to be related to risk of endometrial cancer; risk associated with variants in this gene may vary according to Body mass idnex]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_assertion evidence source_evidence_literature NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_assertion SIO_000772 18437511 NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_assertion wasDerivedFrom lhgdn-20090331 NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_assertion wasGeneratedBy ECO_0000203 NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP187294.RATMVcOrvniPeWvzx_dR4AEMfUnqoLXcXpU_9d84IVv4Y130_provenance.