@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY> .
@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/v4.0.0/void/> .

dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_head {
  this: np:hasAssertion dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion;
    np:hasProvenance dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance;
    np:hasPublicationInfo dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion a np:Assertion .
  
  dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance a np:Provenance .
  
  dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion {
  miriam-gene:2335 a ncit:C16612 .
  
  lld:C0013720 a ncit:C7057 .
  
  dgn-gda:DGN557c470c4d6777d7256b9a242037f889 sio:SIO_000628 miriam-gene:2335, lld:C0013720;
    a sio:SIO_001122 .
}

dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance {
  dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion dcterms:description
      "[Three point mutations in TNX gene were found to be associated with hypermobility type EDS and one of such mutations is the V1195M mutation at the 7th fibronectin Type III domain (TNXfn7).]. 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:20853426;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:05+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: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" .
}