@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY> .
@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:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_head {
  this: np:hasAssertion dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_assertion;
    np:hasProvenance dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_provenance;
    np:hasPublicationInfo dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_assertion a np:Assertion .
  
  dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_provenance a np:Provenance .
  
  dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_assertion {
  miriam-gene:2218 a ncit:C16612 .
  
  lld:C0266464 a ncit:C7057 .
  
  dgn-gda:DGNc2029741f6d6feb2c3f274672e29ca36 sio:SIO_000628 miriam-gene:2218, lld:C0266464;
    a sio:SIO_001121 .
}

dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_provenance {
  dgn-np:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_assertion dcterms:description
      "[Finally, in Fukuyama congenital muscular dystrophy, the deficient fukutin gene product may also be linked to the basal lamina, permitting overmigration of neuronal cells which lead to micropolygyria in the brain, and at the same time cause basal lamina defects in the extracellular matrix of skeletal muscle, which leads to muscular dystrophy.]. 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:10711985;
    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:NP621923.RAAI0PSz4Cb-ncSieW59CbRxnFMofgCp7PH-5LwixfEJY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}