@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg> .
@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:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_head {
  this: np:hasAssertion dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_assertion;
    np:hasProvenance dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_provenance;
    np:hasPublicationInfo dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_assertion a np:Assertion .
  
  dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_provenance a np:Provenance .
  
  dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_assertion {
  miriam-gene:1297 a ncit:C16612 .
  
  lld:C0410538 a ncit:C7057 .
  
  dgn-gda:DGN84010b7061ae94db5c7eaa41955274ae sio:SIO_000628 miriam-gene:1297, lld:C0410538;
    a sio:SIO_001121 .
}

dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_provenance {
  dgn-np:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_assertion dcterms:description
      "[MED, and PSACH mutations, despite displaying phenotypic differences, demonstrated only subtle differences in their cellular viability and mRNA and protein expression of components of the extracellular matrix, including those that interact with COMP.]. 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:20578249;
    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:NP927706.RAbMpuZS-qNB60fInb4g_1uFTIPVn9PSgIhNL0mJdCcEg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}