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- source_evidence_literature type ECO_0000212 NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion description "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion evidence source_evidence_literature NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion SIO_000772 19934113 NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion wasDerivedFrom befree-20140225 NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion wasGeneratedBy ECO_0000203 NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- befree-20140225 importedOn "2014-02-25" NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.