Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_assertion description "[New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_assertion evidence source_evidence_curated NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_assertion SIO_000772 10711710 NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_assertion wasDerivedFrom uniprot-20130724 NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_assertion wasGeneratedBy ECO_0000218 NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP38.RAuuP-B3ljLRPy9R-ghxAvA5c5VxIA-xJcTkEdUqFgHIY130_provenance.