@prefix orcid: . @prefix dc: . @prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_head { this: np:hasAssertion dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_assertion; np:hasProvenance dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_provenance; np:hasPublicationInfo dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_publicationInfo; a np:Nanopublication . dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_assertion a np:Assertion . dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_provenance a np:Provenance . dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_publicationInfo a np:PublicationInfo . } dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_assertion { miriam-gene:2592 a ncit:C16612 . lld:C0268151 a ncit:C7057 . dgn-gda:DGNa18ab3a9ac24cc5945fc9cf002b3ec73 sio:SIO_000628 miriam-gene:2592, lld:C0268151; a sio:SIO_001122 . } dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_provenance { dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_assertion dc:description "[To address this apparent paradox, as well as to investigate the functional significance of the newly identified V151A substitution, all three mutations were recreated by site-directed mutagenesis of the otherwise wild-type human GALT sequence and were expressed both individually and in the appropriate allelic combinations in a GALT-deficient strain of the yeast Saccharomyces cerevisiae.(ABSTRACT TRUNCATED AT 250 WORDS)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:7887417; prov:wasDerivedFrom dgn-void:uniprot-2016; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date . } dgn-np:NP8590.RAkd48W-P1199xa86QeBoQNikAe-SNYkFpim4GPhPFxDA130_publicationInfo { this: dc:created "2016-05-13T12:41:53+02:00"^^xsd:dateTime; dc:rights ; dc:rightsHolder dgn-void:IBIGroup; dc:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X, orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654; pav:createdBy orcid:0000-0003-0169-8159; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }