Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion> ?p ?o ?g. }
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- NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_assertion type Assertion NP476370.RAXUgbK1AqgRh9sil4Xbxal361m15DeHtRcK7IJsAKUlw130_head.
- 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.