@prefix dct: <http://purl.org/dc/terms/> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ> .
@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 np: <http://www.nanopub.org/nschema#> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_head {
  this: np:hasAssertion dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion;
    np:hasProvenance dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance;
    np:hasPublicationInfo dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion a np:Assertion .
  
  dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance a np:Provenance .
  
  dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion {
  miriam-gene:56172 a ncit:C16612 .
  
  lld:C0856830 a ncit:C7057 .
  
  dgn-gda:DGNf267c30cfcacfa8eb0aad356b7ddc1f2 sio:SIO_000628 miriam-gene:56172, lld:C0856830;
    a sio:SIO_001122 .
}

dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance {
  dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion dct:description
      "[These observations represent the fourth and fifth families with heritable CPPD whose disease phenotypes are linked to the CCAL2 locus and who have missense mutations in the amino terminus of ANKH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:13130483;
    prov:wasDerivedFrom dgn-void:uniprot-2016;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}

dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo {
  this: dct:created "2016-05-13T12:41:51+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct: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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}