Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion evidence source_evidence_curated NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion SIO_000772 17676042 NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion wasDerivedFrom uniprot-20150221 NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_assertion wasGeneratedBy ECO_0000218 NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP51.RA3MJ_IbGppLnXhHzf3F2wIyJGbSVgTqOpU28aUldKL1Y130_provenance.