Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion wasGeneratedBy ECO_0000203 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion wasDerivedFrom befree-20140225 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion SIO_000772 21844581 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion evidence source_evidence_literature NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion description "[Although XLG is not a rare disease, there have been no reports of PHKA2 mutations in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.