Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_assertion wasGeneratedBy ECO_0000203 NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_assertion wasDerivedFrom befree-20150227 NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_assertion SIO_000772 23372056 NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_assertion evidence source_evidence_literature NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.
- NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_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." NP674451.RAuAuaThyKD3GPVWOUrS8XC2TREjnv6pPV_eOpkPZ4i6w130_provenance.