Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_assertion description "[These results indicate that a functional defect of the HMCS gene is responsible for classical xanthinuria type II, and that HMCS protein functions to provide a sulfur atom for the molybdenum cofactor of XDH and AO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_assertion evidence source_evidence_literature NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_assertion SIO_000772 11302742 NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_assertion wasDerivedFrom befree-2016 NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_assertion wasGeneratedBy ECO_0000203 NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP314388.RA_CdPfSZMwvuQgoVf4Jj_Ze38L85XR2K53fSO2VfknWU130_provenance.