@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI> .
@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:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_head {
  this: np:hasAssertion dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_assertion;
    np:hasProvenance dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_provenance;
    np:hasPublicationInfo dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_assertion a np:Assertion .
  
  dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_provenance a np:Provenance .
  
  dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_assertion {
  miriam-gene:3914 a ncit:C16612 .
  
  lld:C0014527 a ncit:C7057 .
  
  dgn-gda:DGN56a65acde2fc1b6355620baafd9a5699 sio:SIO_000628 miriam-gene:3914, lld:C0014527;
    a sio:SIO_001121 .
}

dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_provenance {
  dgn-np:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_assertion dcterms:description
      "[Knowledge of the exon-intron organization of the LAMB3 gene will facilitate elucidation of mutations in patients with the junctional forms of epidermolysis bullosa, some of which have been associated with mutations in the laminin 5 genes.]. 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:7774918;
    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:NP772533.RAb9HPNgecsmc5X0EZ-oTYKkt2Trdb3gm155XffQ5LVyI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:47+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" .
}