@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_head {
  this: np:hasAssertion dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion ;
    np:hasProvenance dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance ;
    np:hasPublicationInfo dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion a np:Assertion .
  dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance a np:Provenance .
  dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion {
  miriam-gene:6976 a ncit:C16612 .
  lld:C0004364 a ncit:C7057 .
  dgn-gda:DGN5e710b50cb526cb819dcc579f119c053 sio:SIO_000628 miriam-gene:6976 , lld:C0004364 ;
    a sio:SIO_001121 .
}
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance {
  dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion dcterms:description "[Polymorphisms in T-cell receptor genes can provide important information for the study of the immune response and autoimmune diseases; indeed, rs1800907, a very common single nucleotide polymorphism (SNP) of the TCRB, has been extensively studied in autoimmune diseases in the 1990s using Southern blot analysis and more recently polymerase chain reaction (PCR) and sequencing.]. 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:21599810 ;
    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:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}