Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion> ?p ?o ?g. }
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- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion type Assertion NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_head.
- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion wasGeneratedBy ECO_0000203 NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion wasDerivedFrom befree-2016 NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion SIO_000772 23804752 NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion evidence source_evidence_literature NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_assertion description "[Lesch-Nyhan syndrome (LNS) is a neurodevelopmental disorder caused by mutations in the gene encoding the purine metabolic enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.