@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk> .
@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:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_head {
  this: np:hasAssertion dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion;
    np:hasProvenance dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance;
    np:hasPublicationInfo dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion a np:Assertion .
  
  dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance a np:Provenance .
  
  dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion {
  miriam-gene:650 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN18a1823c343f4fffb36238d8ed87c131 sio:SIO_000628 miriam-gene:650, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance {
  dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion dcterms:description
      "[The abundance of neural stem cells (NSCs) in multiple sclerosis (MS) lesions with extensive astrogliosis suggests that fate factors of NSCs, such as the bone morphogenic protein (BMP) signaling maybe defective in MS. We found an elevated mRNA expression and protein secretion of BMP-2,4,5 but not of BMP-7.]. 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:24080309;
    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:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}