@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk> .
@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:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_head {
  this: np:hasAssertion dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_assertion;
    np:hasProvenance dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_provenance;
    np:hasPublicationInfo dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_assertion a np:Assertion .
  
  dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_provenance a np:Provenance .
  
  dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_assertion {
  miriam-gene:27243 a ncit:C16612 .
  
  lld:C0265218 a ncit:C7057 .
  
  dgn-gda:DGNdaf61ce4221ac25b55a7b2db4d5e4611 sio:SIO_000628 miriam-gene:27243, lld:C0265218;
    a sio:SIO_001121 .
}

dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_provenance {
  dgn-np:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_assertion dcterms:description
      "[The approximately 10 VP1 molecules assembled in the MVM particle harbor in its 142-amino-acid (aa) N-terminal-specific region four clusters of basic amino acids, here called BC1 (aa 6 to 10), BC2 (aa 87 to 90), BC3 (aa 109 to 115), and BC4 (aa 126 to 130), that fit consensus NLS and an NLM placed toward the opposite end of the polypeptide (aa 670 to 680) found to be necessary for VP2 nuclear uptake.]. 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:12072505;
    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:NP177848.RA74vLUgLTS4HR3JGv-0waGCLJ3WdZVDMS_J7FybycwPk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}