@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI> .
@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:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_head {
  this: np:hasAssertion dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion ;
    np:hasProvenance dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance ;
    np:hasPublicationInfo dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion a np:Assertion .
  dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance a np:Provenance .
  dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion {
  miriam-gene:147495 a ncit:C16612 .
  lld:C0023195 a ncit:C7057 .
  dgn-gda:DGN392944e99ef85786c4c4a9708dec1917 sio:SIO_000628 miriam-gene:147495 , lld:C0023195 ;
    a sio:SIO_001121 .
}
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance {
  dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion dcterms:description "[These included membrane cholesterol content (increased in homozygotes with LCAT deficiency), changes in sodium and potassium content and Na+,k+-ATPase activity (the latter being increased in HHS), changes in acetylcholinesterase and sulfhydryl group latency (present in LCAT deficiency, but not in HHS) and 2,3 DPG content (decreased in HHS, normal in LCAT deficiency.]. 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:6246569 ;
    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:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}