@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_head {
  this: np:hasAssertion dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_assertion ;
    np:hasProvenance dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_provenance ;
    np:hasPublicationInfo dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_assertion a np:Assertion .
  dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_provenance a np:Provenance .
  dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_assertion {
  miriam-gene:60506 a ncit:C16612 .
  lld:C3711543 a ncit:C7057 .
  dgn-gda:DGNdd025ce435b8e05660a50ca032b439c1 sio:SIO_000628 miriam-gene:60506 , lld:C3711543 ;
    a sio:SIO_001121 .
}
dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_provenance {
  dgn-np:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_assertion dcterms:description "[The apparent clinical heterogeneity in X-linked CSNB reflects the recently described genetic heterogeneity in which the locus for complete CSNB (CSNB1) was mapped to Xp11.4, and the locus for incomplete CSNB (CSNB2) was refined within Xp11.23 (ref.]. 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:9662400 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP935920.RAiwP2m2Ansm-8yTr8haWXW8aoPaMercPGY81T_b49cV0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:11+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}