Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion description "[ACTN4 mutations seem to account for approximately 4% of familial FSGS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion evidence source_evidence_literature NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion SIO_000772 16251236 NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion wasDerivedFrom befree-20150227 NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion wasGeneratedBy ECO_0000203 NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_provenance.