@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo> .
@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:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_head {
  this: np:hasAssertion dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_assertion;
    np:hasProvenance dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_provenance;
    np:hasPublicationInfo dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_assertion a np:Assertion .
  
  dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_provenance a np:Provenance .
  
  dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C0037274 a ncit:C7057 .
  
  dgn-gda:DGN61c4eb9c6331f3720e4330fefa81d474 sio:SIO_000628 miriam-gene:3918, lld:C0037274;
    a sio:SIO_001121 .
}

dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_provenance {
  dgn-np:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_assertion dcterms:description
      "[The three genes (LAMA3, LAB3 and LAMC2) that encode the anchoring filament protein, laminin 5, may all harbour pathogenetic mutations in the autosomal recessive blistering skin disorder, junctional epidermolysis bullosa (JEB).]. 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:9205497;
    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:NP677744.RA6iw8bKarcA-LHc5oYJfqlxDo2FyOGHM1YmNvG52_yAo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:49+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" .
}