Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion> ?p ?o ?g. }
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- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion type Assertion NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_head.
- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion description "[Recently, another causative gene, CISD2, has been identified in patients with a type of Wolfram syndrome (WS2) resulting in early optic atrophy, diabetes mellitus, deafness, decreased lifespan, but not diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_provenance.
- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion evidence source_evidence_literature NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_provenance.
- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion SIO_000772 22790102 NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_provenance.
- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion wasDerivedFrom befree-20150227 NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_provenance.
- NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_assertion wasGeneratedBy ECO_0000203 NP1002318.RAu3Ioq1NlcTuETowff2I1GvrzN3OUDZDgp_2DUJ_WSc0130_provenance.