@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc> .
@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:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_head {
  this: np:hasAssertion dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion;
    np:hasProvenance dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance;
    np:hasPublicationInfo dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion a np:Assertion .
  
  dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance a np:Provenance .
  
  dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion {
  miriam-gene:2335 a ncit:C16612 .
  
  lld:C0086437 a ncit:C7057 .
  
  dgn-gda:DGN709e2c95035e4ed7ed0914b2fb0eff4b sio:SIO_000628 miriam-gene:2335, lld:C0086437;
    a sio:SIO_001121 .
}

dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance {
  dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion dcterms:description
      "[Since fibronectin is an important adhesive glycoprotein in connective tissue and is required for normal platelet interactions with collagen, we propose that both platelet malfunction and joint hypermobility in this kindred are likely explained by a defective fibronectin.]. 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:7382073;
    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:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}