Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion> ?p ?o ?g. }
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- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion type Assertion NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_head.
- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion description "[Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_provenance.
- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion evidence source_evidence_curated NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_provenance.
- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion SIO_000772 23531866 NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_provenance.
- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion wasDerivedFrom uniprot-2016 NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_provenance.
- NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_assertion wasGeneratedBy ECO_0000218 NP7422.RAch8lxPPCx2XTNC5VH_8PirFOfxkePkN1fHldaES4Hfw130_provenance.