Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_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." NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_assertion evidence source_evidence_literature NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_assertion SIO_000772 11302742 NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_assertion wasDerivedFrom befree-20140225 NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_assertion wasGeneratedBy ECO_0000203 NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP838825.RA7NdFZ2I0l6iaLR3dY_OBQcdGH3-o0noz0drp4czIYY4130_provenance.