Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion> ?p ?o ?g. }
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- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion type Assertion NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_head.
- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion wasGeneratedBy ECO_0000203 NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_provenance.
- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion wasDerivedFrom befree-20150227 NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_provenance.
- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion SIO_000772 12659814 NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_provenance.
- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion evidence source_evidence_literature NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_provenance.
- NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_assertion description "[A mutation has been identified in the Rab3A-interacting molecule (RIM1) gene in CORD7, an autosomal dominant cone-rod dystrophy that localises to chromosome 6q14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662616.RAA1AGuzp-CWYv7ShDppOLVR7-09Wy-D0vbXQyX4Q1qtk130_provenance.