Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1089443.RAWI8s3v29fAbWWjDyA3lhrCq7Dkeqn1Iyd5Xjx1q6aj4130_provenance.
- 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.