Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_assertion description "[Missense mutations of ACTA1 cause dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_assertion evidence source_evidence_curated NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_assertion SIO_000772 15520409 NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_assertion wasDerivedFrom uniprot-20130724 NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_assertion wasGeneratedBy ECO_0000218 NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP149.RARr6MkLjulr1Nxfz7zt_R0l1ccqhySsNZp5uXitkeozw130_provenance.