@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto> .
@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:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_head {
  this: np:hasAssertion dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion ;
    np:hasProvenance dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance ;
    np:hasPublicationInfo dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion a np:Assertion .
  dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance a np:Provenance .
  dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion {
  miriam-gene:6439 a ncit:C16612 .
  lld:C0020630 a ncit:C7057 .
  dgn-gda:DGN73a1a91b362721e086854b2d153f5ca8 sio:SIO_000628 miriam-gene:6439 , lld:C0020630 ;
    a sio:SIO_001121 .
}
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance {
  dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_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:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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" .
}