@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0> .
@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:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_head {
  this: np:hasAssertion dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_assertion ;
    np:hasProvenance dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_provenance ;
    np:hasPublicationInfo dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_assertion a np:Assertion .
  dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_provenance a np:Provenance .
  dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_assertion {
  miriam-gene:4015 a ncit:C16612 .
  lld:C0022716 a ncit:C7057 .
  dgn-gda:DGN580750f37d34216cec9afdffb4723ab4 sio:SIO_000628 miriam-gene:4015 , lld:C0022716 ;
    a sio:SIO_001121 .
}
dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_provenance {
  dgn-np:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_assertion dcterms:description "[We report here that the amount of lysyl oxidase mRNA, as studied by Northern blotting, and the number of lysyl oxidase mRNA molecules per picogram of RNA, as determined by a quantitative PCR method, were decreased in three cultured skin fibroblast lines from patients with the Menkes syndrome and two from patients with the occipital horn syndrome compared with four control cell lines.]. 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:8638917 ;
    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:NP664350.RA0INI5tBCzSDNMlz4FJYfujgRE_LIQyUCFSD_NhXLil0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}