@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:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_head { this: np:hasAssertion dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_assertion; np:hasProvenance dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_provenance; np:hasPublicationInfo dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_publicationInfo; a np:Nanopublication . dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_assertion a np:Assertion . dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_provenance a np:Provenance . dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_publicationInfo a np:PublicationInfo . } dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_assertion { miriam-gene:6520 a ncit:C16612 . lld:C0026769 a ncit:C7057 . dgn-gda:DGN1c38d0b3c1b9f10eebae3b61613925f5 sio:SIO_000628 miriam-gene:6520, lld:C0026769; a sio:SIO_001121 . } dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_provenance { dgn-np:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_assertion dcterms:description "[A haplotype marker consisting of three biallelic restriction fragment length polymorphism (RFLP) loci from the VH-2 variable gene family was examined in 124 families with sibling pairs concordant for multiple sclerosis, 178 unrelated patients and 159 unaffected controls to investigate the role of the immunoglobulin heavy chain gene cluster in susceptibility to multiple sclerosis.]. 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:8568530; 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:NP1346023.RAgHfc-m5E3DTzD7-J_9tjNhLzokrPrlx9ez2KQLpjb_o130_publicationInfo { this: dcterms:created "2016-05-13T12:51:56+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" . }