Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_assertion description "[A missense mutation (Trp 26-->Arg) in exon 3 of the apolipoprotein CII gene in a patient with apolipoprotein CII deficiency (apo CII-Wakayama).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_assertion evidence source_evidence_curated NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_assertion SIO_000772 8323539 NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_assertion wasDerivedFrom uniprot-20150221 NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_assertion wasGeneratedBy ECO_0000218 NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP895.RA5Bu0KFocuthWRmF35ANys3zTygRGXhB__IwlUcHTYpE130_provenance.