Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_assertion description "[Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_assertion evidence source_evidence_curated NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_assertion SIO_000772 12649162 NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_assertion wasDerivedFrom uniprot-2016 NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_assertion wasGeneratedBy ECO_0000218 NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2586.RAzP2CEXx0Tw6c5ThhUkItuJifsqJa0UnXt5ElhgnN94g130_provenance.