Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion> ?p ?o ?g. }
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- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion type Assertion NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_head.
- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion description "[Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_provenance.
- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion evidence source_evidence_curated NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_provenance.
- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion SIO_000772 16960802 NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_provenance.
- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion wasDerivedFrom uniprot-2016 NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_provenance.
- NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_assertion wasGeneratedBy ECO_0000218 NP4695.RAD1QcSCTQaq8h3ZYiNle2GOnbuPDSI1hWLl1MPOqlrtI130_provenance.