@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA> .
@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:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_head {
  this: np:hasAssertion dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_assertion;
    np:hasProvenance dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_provenance;
    np:hasPublicationInfo dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_assertion a np:Assertion .
  
  dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_provenance a np:Provenance .
  
  dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_assertion {
  miriam-gene:2778 a ncit:C16612 .
  
  lld:C0016063 a ncit:C7057 .
  
  dgn-gda:DGN0ad195c114576382506885e9e3c6309c sio:SIO_000628 miriam-gene:2778, lld:C0016063;
    a sio:SIO_001121 .
}

dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_provenance {
  dgn-np:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_assertion dcterms:description
      "[Results from the initial analysis of the series indicate five main points: (1) Significant diagnostic pitfalls affect the diagnosis of MFD and, to a lesser extent, PFD in orthopedic centers and allied radiology and pathology facilities, which may be circumvented by the adoption of stringent diagnostic criteria, and in some cases by the analysis of FD-associated GNAS1 mutations.]. 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:12703030;
    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:NP319895.RAy0A4Rzcaj1vpa2nS7YdhiRGJOnRjUSIWdKA1iy1enTA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:05+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" .
}