@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:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_head { this: np:hasAssertion dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_assertion; np:hasProvenance dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_provenance; np:hasPublicationInfo dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_publicationInfo; a np:Nanopublication . dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_assertion a np:Assertion . dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_provenance a np:Provenance . dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_publicationInfo a np:PublicationInfo . } dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_assertion { miriam-gene:10986 a ncit:C16612 . lld:C0162538 a ncit:C7057 . dgn-gda:DGNc7f1e1e6ff77b1738902784c3b1d522a sio:SIO_000628 miriam-gene:10986, lld:C0162538; a sio:SIO_001121 . } dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_provenance { dgn-np:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_assertion dcterms:description "[Here we show an increased allele sharing at 6p21 in affected members of 83 multiplex IgAD/CVID pedigrees and demonstrate, using transmission/diseqilibrium tests, family-based associations indicating the presence of a predisposing locus, designated `IGAD1,` in the proximal part of the major histocompatibility complex (MHC).]. 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:10090895; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP848258.RA0dTEFIWuGUmbuP5ARA3WGx4JXBqthDlHOP3ZcW5NpB4130_publicationInfo { this: dcterms:created "2014-10-02T12:40:38+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }