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- source_evidence_literature type ECO_0000212 NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_assertion wasGeneratedBy ECO_0000203 NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_assertion wasDerivedFrom befree-20140225 NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_assertion SIO_000772 18974381 NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_assertion evidence source_evidence_literature NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_assertion description "[We examined the association of common ANGPTL4 variants with CHD traits and risk in 5 studies (13,527 individuals).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP227794.RAqTpg6idEtX9uSVr0NhnFue2A_QkNfToDPloy4YHcksw130_provenance.