Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_assertion evidence source_evidence_curated NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_assertion SIO_000772 23603762 NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_assertion wasDerivedFrom ctd_human-20150221 NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_assertion wasGeneratedBy ECO_0000218 NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP20272.RAAM7C4hJsVb7WjlnO303LpFOFf3EKoINIwr9nSnHvaIA130_provenance.