@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c> .
@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:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_head {
  this: np:hasAssertion dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_assertion ;
    np:hasProvenance dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_provenance ;
    np:hasPublicationInfo dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_assertion a np:Assertion .
  dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_provenance a np:Provenance .
  dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  lld:C0684249 a ncit:C7057 .
  dgn-gda:DGNcd8f1b23d336e3172c287de482655d96 sio:SIO_000628 miriam-gene:5265 , lld:C0684249 ;
    a sio:SIO_001121 .
}
dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_provenance {
  dgn-np:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_assertion dcterms:description "[The lung represents an attractive target organ for somatic gene therapy strategy in that, (1) it is easily accessible by vectors, (2) most frequent hereditary disorders, cystic fibrosis (CF) and alpha1-antitrypsin deficiency (alpha1AT), occur in the lung, and (3) carcinoma of the lung is apparently a most common cause of death in humans.]. 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:11899243 ;
    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:NP400563.RABYcXNKPA2BlMgbquyJckN1GdG2fjXMZOMmd8VovpN1c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+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" .
}