Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_assertion description "[Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_assertion evidence source_evidence_curated NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_assertion SIO_000772 10102298 NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_assertion wasDerivedFrom uniprot-20130724 NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_assertion wasGeneratedBy ECO_0000218 NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5547.RA1fBOujliisB0l-ppRuLAsimw2lTmR3nTM5qdYYz_Otk130_provenance.