Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion> ?p ?o ?g. }
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- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion type Assertion NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_head.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion wasGeneratedBy ECO_0000203 NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion wasDerivedFrom befree-2016 NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion SIO_000772 23372056 NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_assertion evidence source_evidence_literature NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.
- NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_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." NP1049083.RABPUjeRBifZIUjLL7P-1p-c2kIcpwNbyExdZZUXjDf2w130_provenance.