Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_assertion description "[To identify mutations in the RPGR and RP2 genes from Chinese families with X-linked retinitis pigmentosa (XLRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_assertion evidence source_evidence_literature NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_assertion SIO_000772 20021257 NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_assertion wasDerivedFrom befree-20150227 NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_assertion wasGeneratedBy ECO_0000203 NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988552.RA31wa-wEpSgzoevSGs2MVwQxD8B1Iz4TcizVJhXtGiCk130_provenance.