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- source_evidence_literature type ECO_0000212 NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_assertion evidence source_evidence_literature NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_assertion SIO_000772 10447258 NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_assertion wasDerivedFrom befree-20150227 NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_assertion wasGeneratedBy ECO_0000203 NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985417.RAYm1FPMCceuEFVc_YE4hke4p1iG96yyvTe5r3BYfa3Zk130_provenance.