@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4> .
@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:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_head {
  this: np:hasAssertion dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_assertion ;
    np:hasProvenance dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_provenance ;
    np:hasPublicationInfo dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_provenance a np:Provenance .
  dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_assertion {
  miriam-gene:503618 a ncit:C16612 .
  lld:C0024115 a ncit:C7057 .
  dgn-gda:DGNe59efcb1127b76c584bbe5781b4c87e2 sio:SIO_000628 miriam-gene:503618 , lld:C0024115 ;
    a sio:SIO_001121 .
}
dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_provenance {
  dgn-np:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_assertion dcterms:description "[Given the higher complexity found in the genomic organization of the DEFB4 and DEFB104 genes, association studies with CF lung disease severity were performed only for frequent polymorphisms located in DEFB1.]. 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:15820309 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  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:NP761330.RAyVqma6q7Tm5MSNtOTQYKBluOZZ-iY3H-EfS8lbaYBZ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}