@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:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_head { this: np:hasAssertion dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_assertion; np:hasProvenance dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_provenance; np:hasPublicationInfo dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_publicationInfo; a np:Nanopublication . dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_assertion a np:Assertion . dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_provenance a np:Provenance . dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_publicationInfo a np:PublicationInfo . } dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_assertion { miriam-gene:9097 a ncit:C16612 . lld:C0002726 a ncit:C7057 . dgn-gda:DGN8d77f450b7f67ce1af62ca3d7c73cda1 sio:SIO_000628 miriam-gene:9097, lld:C0002726; a sio:SIO_001121 . } dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_provenance { dgn-np:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_assertion dcterms:description "[MBL2 structural gene polymorphisms at codon 52 (CGT-->TGT, Arg-->Cys; D), codon 54 (GGC-->GAC, Gly-->Asp; B) and codon 57 (GGA-->GAA, Gly--> Glu; C), and MBL2 promoter region polymorphism at position -221 (G-->C) were examined in 57 patients with RA complicated by biopsy-proven reactive amyloidosis and 51 control RA patients without amyloid.]. 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:17875183; 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:NP815014.RAMnWVLP7CffyFx6Tb3BFQxppblADL3uXe9M9yj3koX2g130_publicationInfo { this: dcterms:created "2015-08-25T14:45:53+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" . }