@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:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_head { this: np:hasAssertion dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_assertion; np:hasProvenance dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_provenance; np:hasPublicationInfo dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_publicationInfo; a np:Nanopublication . dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_assertion a np:Assertion . dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_provenance a np:Provenance . dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_publicationInfo a np:PublicationInfo . } dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_assertion { miriam-gene:7124 a ncit:C16612 . lld:C0014072 a ncit:C7057 . dgn-gda:DGNf6a3fa1545c05db6b44632cdf9563c7c sio:SIO_000628 miriam-gene:7124, lld:C0014072; a sio:SIO_001121 . } dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_provenance { dgn-np:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_assertion dcterms:description "[Recently, it has been reported that the TNF receptor (TNFR) II plays an essential role in the pathology and progression of experimental autoimmune encephalomyelitis, an animal model of MS. To investigate whether TNFR II polymorphisms influence susceptibility and/or clinical progression of MS, genomic DNA of 321 samples of the Austrian Genetics in MS study group and DNA of 174 platelet donors, who served as healthy controls, were genotyped for five polymorphic sites in the TNFR II gene: exon 6 nucleotide (nt) 676*T-->G, exon 6 nt 783*G-->A (both are associated with non-conserved amino acid substitution), exon 10 nt 1663*G-->A, exon 10 nt 1668*T-->G, and exon 10 nt 1690*T-->C (all of which are located in the 3' non-coding region of the gene).]. 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:14651520; 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:NP422955.RACB7OqU8kn-F4WnVjaPpulmHO-wJoyF89FYVdf8o0nPY130_publicationInfo { this: dcterms:created "2016-05-13T12:44:57+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" . }