@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:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_head { this: np:hasAssertion dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_assertion; np:hasProvenance dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_provenance; np:hasPublicationInfo dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_publicationInfo; a np:Nanopublication . dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_assertion a np:Assertion . dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_provenance a np:Provenance . dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_publicationInfo a np:PublicationInfo . } dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_assertion { miriam-gene:1280 a ncit:C16612 . lld:C0409957 a ncit:C7057 . dgn-gda:DGN27ec110c525d7a68d54cf0cc9baa6884 sio:SIO_000628 miriam-gene:1280, lld:C0409957; a sio:SIO_001121 . } dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_provenance { dgn-np:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_assertion dcterms:description "[Nevertheless, association studies of affected sibling pairs and nuclear families, using candidate gene and genome wide screening and transmission disequilibrium testing, suggest no association with candidates such as COL2A1 (responsible for some rare monogenic syndromes of premature generalized OA) but possible associations, currently not isolated, on chromosome 2q.]. 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:11156501; 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:NP319526.RAtLaHw4y-8-le3FnQzryGUrAbG8m-nylmIwvsufAYht8130_publicationInfo { this: dcterms:created "2015-08-25T14:40:43+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" . }