@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0> .
@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:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_head {
  this: np:hasAssertion dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_assertion ;
    np:hasProvenance dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_provenance ;
    np:hasPublicationInfo dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_assertion a np:Assertion .
  dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_provenance a np:Provenance .
  dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_assertion {
  miriam-gene:23545 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
  dgn-gda:DGN317d9addafccc13a9fb3988e68f7a31c sio:SIO_000628 miriam-gene:23545 , lld:C0000768 ;
    a sio:SIO_001121 .
}
dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_provenance {
  dgn-np:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_assertion dcterms:description "[The autosomal recessive form of type II cutis laxa (ARCL II) is characterized by the appearance of redundant, inelastic skin with wrinkling, an aged look and additional variable systemic involvement including intrauterine growth retardation, failure to thrive, developmental delay, dysmorphism, osseous abnormality, and CNS manifestations.]. 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:21567914 ;
    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:NP521826.RAHipk9GVS-PdKNjHP5j8gdxYB_SgLPzq3nZQwLct7Rt0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+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" .
}