@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 dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_head { this: np:hasAssertion dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_assertion; np:hasProvenance dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_provenance; np:hasPublicationInfo dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_publicationInfo; a np:Nanopublication . dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_assertion a np:Assertion . dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_provenance a np:Provenance . dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_publicationInfo a np:PublicationInfo . } dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_assertion { miriam-gene:240 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGN67bb0cd284ab0dd08eda9ff7c12810a5 sio:SIO_000628 miriam-gene:240, lld:C0004096; a sio:SIO_001122 . } dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_provenance { dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_assertion dcterms:description "[A polymorphism study that examined nine single-nucleotide polymorphisms of five leukotriene-related genes [ALOX5 (encoding 5-lipoxygenase), ALOX5AP (5-lipoxygenase-activating protein), PTGS2 (cyclooxygenase 2), LTC4S (leukotriene C4 synthase), and CYSLTR1 (cysteinyl leukotriene receptor 1)] found that promoter polymorphisms of ALOX5 (-1708A>G) and CYSLTR1 (-634C>T) were significantly different between aspirin-intolerant asthma and aspirin-induced urticaria/angioedema, suggesting different contributions to the lipoxygenase pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:16825866; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP558680.RA1H2KBa0gKgXLHH5E-MBBr8XtdgE9dmjDrFEnBD_VdwU130_publicationInfo { this: dcterms:created "2016-05-13T12:45:58+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }