@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o> .
@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:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_head {
  this: np:hasAssertion dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion;
    np:hasProvenance dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance;
    np:hasPublicationInfo dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion a np:Assertion .
  
  dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance a np:Provenance .
  
  dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion {
  miriam-gene:199699 a ncit:C16612 .
  
  lld:C0271994 a ncit:C7057 .
  
  dgn-gda:DGNe6e7bf953d9edb4df4ec09d358a35a12 sio:SIO_000628 miriam-gene:199699, lld:C0271994;
    a sio:SIO_001121 .
}

dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance {
  dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion dcterms:description
      "[Gel mobility shift assays with nuclear extract from K562 cells (which contain both Sp1 and SSP) demonstrate preferential binding of SSP to the SSE and HPFH sites under conditions in which probe was limiting.]. 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:7684493;
    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:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:01+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" .
}