Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion> ?p ?o ?g. }
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- NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_assertion type Assertion NP222100.RANiDmVkanb-cIrHpgdbgMiPk3S0CckKp0JXKm8pOKiho130_head.
- 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.