Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_assertion wasGeneratedBy ECO_0000203 NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_assertion wasDerivedFrom befree-20150227 NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_assertion SIO_000772 7655856 NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_assertion evidence source_evidence_literature NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.
- NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_assertion description "[Among glycolytic enzyme defects, hexokinase (ATP: D-hexose 6-phosphotransferase, EC 2.7.1.1; HK) deficiency is a very rare disease where the predominant clinical effect is nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450396.RAeA3rPS4DnElvAv-mUIWRn1PJw7yuEDY6frZ3o2U_HE8130_provenance.