@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_head {
  this: np:hasAssertion dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_assertion ;
    np:hasProvenance dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_provenance ;
    np:hasPublicationInfo dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_assertion a np:Assertion .
  dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_provenance a np:Provenance .
  dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_assertion {
  miriam-gene:7124 a ncit:C16612 .
  lld:C0034734 a ncit:C7057 .
  dgn-gda:DGN39756827adc8f4bbe5ee84a9a06c0612 sio:SIO_000628 miriam-gene:7124 , lld:C0034734 ;
    a sio:SIO_001121 .
}
dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_provenance {
  dgn-np:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_assertion dcterms:description "[When the SLE group was analyzed according to presentation of certain clinical features, photosensitivity and Raynaud's phenomenon, the frequency of these alleles (TNF a2, b3 and d2) were also significantly increased.]. 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:9098928 ;
    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:NP745195.RAqRxW38b3zvhKHxyifFrr3pSd39Fc0Ygy0vpTYIsZVG4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:09+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}