Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_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." NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_assertion evidence source_evidence_curated NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_assertion SIO_000772 23603762 NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_assertion wasDerivedFrom uniprot-2016 NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_assertion wasGeneratedBy ECO_0000218 NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7455.RAum83li0xgwfdujhxMpHW0UsBcDfT4WFJY7ZgfT5w_Fw130_provenance.