@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0> .
@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:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_head {
  this: np:hasAssertion dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_assertion ;
    np:hasProvenance dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_provenance ;
    np:hasPublicationInfo dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_assertion a np:Assertion .
  dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_provenance a np:Provenance .
  dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_assertion {
  miriam-gene:450095 a ncit:C16612 .
  lld:C0746102 a ncit:C7057 .
  dgn-gda:DGNd69ff8374db1e9e30ea9aa62d1e74421 sio:SIO_000628 miriam-gene:450095 , lld:C0746102 ;
    a sio:SIO_001121 .
}
dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_provenance {
  dgn-np:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_assertion dcterms:description "[In the musculoskeletal system, likelihood is high for avascular necrosis of the femoral humeral head, as a consequence of skeletal infarcts, and also for leg ulceration and osteomyelitis; in the eyes, the incidence of proliferative retinopathy is high; in the urinary tract, dehydration is common, and causes for renal failure are many; in the pulmonary system, pneumonia is of prime concern, as are sickle cell chest syndrome (from occlusion within the microvasculature of the lung) and the deadly sickle cell chronic lung disease, for which pulmonary function tests are important in early asymptomatic stages.]. 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:8557548 ;
    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:NP900426.RAnJ-QTfLqnmV1JTgMrYCTIT6JUJZaeGiXn5ZUOy6Jvr0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}