@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ> .
@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:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_head {
  this: np:hasAssertion dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_assertion ;
    np:hasProvenance dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_assertion a np:Assertion .
  dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_provenance a np:Provenance .
  dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_assertion {
  miriam-gene:50509 a ncit:C16612 .
  lld:C0013720 a ncit:C7057 .
  dgn-gda:DGN2a8bab3c15627c2ca150af8d12c98153 sio:SIO_000628 miriam-gene:50509 , lld:C0013720 ;
    a sio:SIO_001121 .
}
dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_provenance {
  dgn-np:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_assertion dcterms:description "[This distribution, and the association of alpha1(V), alpha2(V), and alpha3(V) chains in heterotrimers, suggests the human alpha3(V) gene COL5A3 as a candidate locus for at least some cases of classical EDS in which the alpha1(V) and alpha2(V) genes have been excluded, and for at least some cases of the hypermobility type of EDS, a condition marked by gross joint laxity and chronic musculoskeletal pain.]. 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:10722718 ;
    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:NP467499.RAYU5I_k-Trae_Lr9_sXTUUCUMqkUuV8e12tvaYOX30jQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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" .
}