Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_assertion description "[Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_assertion evidence source_evidence_curated NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_assertion SIO_000772 15336687 NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_assertion wasDerivedFrom uniprot-20130724 NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_assertion wasGeneratedBy ECO_0000218 NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP152.RAEuc4RTSwh8uDm7x1CzOkwQaO9PBRuZ7WhGLad15aIys130_provenance.