@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs> .
@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:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_head {
  this: np:hasAssertion dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_assertion;
    np:hasProvenance dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_provenance;
    np:hasPublicationInfo dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_publicationInfo a
      np:PublicationInfo .
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dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_assertion {
  miriam-gene:147495 a ncit:C16612 .
  
  lld:C0023195 a ncit:C7057 .
  
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dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_provenance {
  dgn-np:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_assertion dcterms:description
      "[In the hope of deriving some information concerning the interrelationship between the structural and functional abnormalities, we have used the spin probe 5-doxyl stearic acid to investigate the temperature-dependent fluidity properties of red cells from two patients with a hereditary hemolytic syndrome (HHS) whose red cells are also characterized by qualitatively similar alterations in phosphatidylcholine and phosphatidylethanolamine but, unlike those in LCAT deficiency, have relatively normal levels of membrane cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP253771.RA7x_r98llciWF04JXZfHZpxbHpXawme7GuBUpVTQ9ROs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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;
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