Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion wasGeneratedBy ECO_0000203 NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion wasDerivedFrom befree-20140225 NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion SIO_000772 23583749 NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion evidence source_evidence_literature NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion description "[Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate uridylyltransferase (GALT; EC 2.7.7.12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_provenance.