@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c> .
@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:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_head {
  this: np:hasAssertion dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion ;
    np:hasProvenance dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance ;
    np:hasPublicationInfo dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion a np:Assertion .
  dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance a np:Provenance .
  dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion {
  miriam-gene:1281 a ncit:C16612 .
  lld:C0042143 a ncit:C7057 .
  dgn-gda:DGNf475bc28d80770f9e78e65887a177c87 sio:SIO_000628 miriam-gene:1281 , lld:C0042143 ;
    a sio:SIO_001121 .
}
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance {
  dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion dcterms:description "[The vascular type of the Ehlers-Danlos syndrome (Ehlers-Danlos syndrome type IV, EDS IV; OMIM #130050) is a rare connective tissue disorder with autosomal dominant transmission caused by mutations in the COL3A1 gene resulting in increased fragility of connective tissue with arterial, intestinal, and uterine ruptures and premature death.]. 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:23489429 ;
    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:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:10+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" .
}