Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion> ?p ?o ?g. }
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- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion type Assertion NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_head.
- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion wasGeneratedBy ECO_0000203 NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.
- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion wasDerivedFrom befree-20140225 NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.
- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion SIO_000772 23372056 NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.
- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion evidence source_evidence_literature NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.
- NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465622.RAtzw5iOWgj5Jkm_dEFvM0Cwsgl0UG3rFqSuMR_KSkCZg130_provenance.