Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion> ?p ?o ?g. }
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- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion type Assertion NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_head.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion wasGeneratedBy ECO_0000203 NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion wasDerivedFrom befree-20150227 NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion SIO_000772 23372056 NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_assertion evidence source_evidence_literature NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.
- NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_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." NP988544.RAymO0cWefa8BpzO0zawChfo5IjJnb5IdaAWW7msqJIgo130_provenance.