Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_assertion wasGeneratedBy ECO_0000203 NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_assertion wasDerivedFrom befree-20150227 NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_assertion SIO_000772 21844581 NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_assertion evidence source_evidence_literature NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.
- NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_assertion description "[A novel PHKA2 gross deletion mutation in a Korean patient with X-linked liver glycogenosis type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619608.RAUrmxCfm2gVHwdhTrzoc_25KPJgxKX2wFR2atdSdoChA130_provenance.