@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc> .
@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:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_head {
  this: np:hasAssertion dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_assertion ;
    np:hasProvenance dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_provenance ;
    np:hasPublicationInfo dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_assertion a np:Assertion .
  dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_provenance a np:Provenance .
  dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_assertion {
  miriam-gene:6439 a ncit:C16612 .
  lld:C0035220 a ncit:C7057 .
  dgn-gda:DGN4e9da23a6926b2e3cadd5d1c0ab8681b sio:SIO_000628 miriam-gene:6439 , lld:C0035220 ;
    a sio:SIO_001121 .
}
dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_provenance {
  dgn-np:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_assertion dcterms:description "[Although the relative abundance of the deletion form of SP-B mRNA remains constant among normal lungs, it is found with relatively higher abundance in the lungs of some individuals with diseases such as congenital alveolar proteinosis, respiratory distress syndrome, bronchopulmonary dysplasia, alveolar capillary dysplasia and hypophosphatasia.]. 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:10493923 ;
    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:NP774542.RAfLAoAhvguIyteHLCrHmMuQ4FW0-OuFhrBz8g4IHjYfc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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" .
}