@prefix np: <http://www.nanopub.org/nschema#> .
@prefix this: <http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs> .
@prefix sub: <http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#RAb5oaamdOKxwOjo1Y3wogV_xSwsmjl-uTfciTSncoUCs.> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix opm: <http://purl.org/net/opmv/ns#> .
@prefix pav: <http://swan.mindinformatics.org/ontologies/1.2/pav/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

sub:NanoPub_1_Head {
  this: np:hasAssertion sub:NanoPub_1_Assertion;
    np:hasProvenance sub:NanoPub_1_Provenance;
    np:hasPublicationInfo sub:NanoPub_1_Pubinfo;
    a np:Nanopublication .
}

sub:NanoPub_1_Assertion {
  sub:Association_1 sio:has-measurement-value sub:Association_1_p_value;
    sio:refers-to <http://bio2rdf.org/geneid:55835>, <http://bio2rdf.org/omim:210600>;
    a sio:statistical-association;
    rdfs:comment """This association has p-value of 0.00066, has attribute gene CENPJ (Entrenz gene id 55835)
        and attribute disease Seckel Syndrome (OMIM 210600)."""@en .
  
  sub:Association_1_p_value sio:has-value "0.0000656211037469712"^^xsd:float;
    a sio:probability-value .
}

sub:NanoPub_1_Provenance {
  sub:NanoPub_1_Assertion opm:wasDerivedFrom <http://rdf.biosemantics.org/vocabularies/text_mining/gene_disease_concept_profiles_1980_2010>;
    opm:wasGeneratedBy <http://rdf.biosemantics.org/vocabularies/text_mining/gene_disease_concept_profiles_matching_1980_2010> .
}

sub:NanoPub_1_Pubinfo {
  this: dcterms:created "2012-03-28T11:32:30.758274Z"^^xsd:dateTime;
    dcterms:rights <http://creativecommons.org/licenses/by/3.0/>;
    dcterms:rightsHolder <http://biosemantics.org>;
    pav:authoredBy <http://www.researcherid.com/rid/B-5927-2012>, <http://www.researcherid.com/rid/B-6035-2012>;
    pav:createdBy <http://www.researcherid.com/rid/B-5852-2012> .
}