@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ> .
@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:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_head {
  this: np:hasAssertion dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_assertion;
    np:hasProvenance dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_provenance;
    np:hasPublicationInfo dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_assertion a np:Assertion .
  
  dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_provenance a np:Provenance .
  
  dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_assertion {
  miriam-gene:1778 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGNe6bc83fc72081218f463825857e1029c sio:SIO_000628 miriam-gene:1778, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_provenance {
  dgn-np:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_assertion dcterms:description
      "[The families have been studied for linkage of asthma and atopy to loci on chromosome 8p following the observation that one family suggested preliminary evidence of linkage to an anonymous hypervariable locus cloned from a DNA fingerprint and mapped to 8pter-p22.]. 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:7812888;
    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:NP836607.RAbtmPEjFaXK_cOvxvNff9G8AY13eV2R1rZkTQraciiIQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}