@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4> .
@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:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_head {
  this: np:hasAssertion dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_assertion;
    np:hasProvenance dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_provenance;
    np:hasPublicationInfo dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_assertion a np:Assertion .
  
  dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_provenance a np:Provenance .
  
  dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  
  lld:C0028043 a ncit:C7057 .
  
  dgn-gda:DGN0b25759c4728b3f54010f9e132e8b486 sio:SIO_000628 miriam-gene:3356, lld:C0028043;
    a sio:SIO_001121 .
}

dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_provenance {
  dgn-np:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_assertion dcterms:description
      "[The polymorphism in HTR2A (102T/C, -1438A/G) was identified by means of the polymerase chain reaction followed by restriction fragment length polymorphism, and the Fagerstrom Test for Nicotine Dependence was used to determine the extent of smoking behavior.]. 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:15564892;
    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:NP895322.RAy99PM0q3mG7n7gm13EcbFdyvg3NqfS77vit7lSwd7L4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:10+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" .
}