Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_assertion description "[The purpose of the study was to evaluate the GPR143 gene (G-protein coupled receptor 143) in a Chinese three-generation family with OA1, including four carriers and a proband with clinical features of X-linked ocular albinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_assertion evidence source_evidence_literature NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_assertion SIO_000772 19123159 NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_assertion wasDerivedFrom befree-20150227 NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_assertion wasGeneratedBy ECO_0000203 NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601258.RAKTDQXDKskv2iJwG3LAYc_IMV_5Hh1NsXIab4oAIJ_cc130_provenance.