@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:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_head { this: np:hasAssertion dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_assertion; np:hasProvenance dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_provenance; np:hasPublicationInfo dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_publicationInfo; a np:Nanopublication . dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_assertion a np:Assertion . dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_provenance a np:Provenance . dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_publicationInfo a np:PublicationInfo . } dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_assertion { miriam-gene:162282 a ncit:C16612 . lld:C0026769 a ncit:C7057 . dgn-gda:DGN1d651a717ee84067eba5035c88a7f583 sio:SIO_000628 miriam-gene:162282, lld:C0026769; a sio:SIO_001122 . } dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_provenance { dgn-np:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_assertion dcterms:description "[Replication extended to the following polymorphisms: PKN2 (rs305217), GTF2B (rs7538427), EPHA4 (rs1517440), YTHDF3 (rs12115114), ANKFN1 (rs17758761) and PTPRM (rs4798571), which did not reach the threshold of significance in a follow-up of the first genome-wide association study (GWAS) conducted in multiple sclerosis; TMEM39A (rs1132200), which appeared as a newly identified susceptibility gene in the same study; a gene previously reaching GWAS significance in Italy, CBLB (rs9657904); IL12B (rs6887695, rs10045431), a susceptibility gene shared by diverse autoimmune diseases and, finally, another gene showing inconclusive association with multiple sclerosis, CNR1 (rs1049353).]. 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:22194214; 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:NP977361.RAEBtxY_MiuqZujWYXrS3hNDa3d5a8m8BCwNAa2OFe6rM130_publicationInfo { this: dcterms:created "2015-08-25T14:47:37+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" . }