@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:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_head { this: np:hasAssertion dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_assertion; np:hasProvenance dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_provenance; np:hasPublicationInfo dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_publicationInfo; a np:Nanopublication . dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_assertion a np:Assertion . dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_provenance a np:Provenance . dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_publicationInfo a np:PublicationInfo . } dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_assertion { miriam-gene:3553 a ncit:C16612 . lld:C0018784 a ncit:C7057 . dgn-gda:DGNc74aabe3f4588549760e4fbfb545d8d5 sio:SIO_000628 miriam-gene:3553, lld:C0018784; a sio:SIO_001122 . } dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_provenance { dgn-np:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_assertion dcterms:description "[The genotypes of interleukin 1A (IL1A) (-889C/T; rs1800587) and interleukin 1B (IL1B) (-511C/T; rs16944) were determined using an allele-specific primer-polymerase chain reaction method in 72 patients with SSNHL, 68 patients with Ménière's disease, and 2202 control subjects living almost in the same area as the patients.]. 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:21385326; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP489213.RAtLjGEqqt-FgezEpBXhjiQ9elfKaZG8lTqGjQp_FpH6U130_publicationInfo { this: dcterms:created "2015-08-25T14:42:28+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }