@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk> .
@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:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_head {
  this: np:hasAssertion dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_assertion;
    np:hasProvenance dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_provenance;
    np:hasPublicationInfo dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_assertion a np:Assertion .
  
  dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_provenance a np:Provenance .
  
  dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_assertion {
  miriam-gene:4153 a ncit:C16612 .
  
  lld:C0745287 a ncit:C7057 .
  
  dgn-gda:DGNd9667b0f703b710c918e7ce3fd886c70 sio:SIO_000628 miriam-gene:4153, lld:C0745287;
    a sio:SIO_001121 .
}

dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_provenance {
  dgn-np:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_assertion dcterms:description
      "[This study focused on four polymorphisms in the mannose binding lectin gene (MBL2) and assessed their significance in tubal damage and female fertility by comparing genotype frequencies among 388 controls and women with tubal factor infertility (n=155) or previous ectopic pregnancy (n=178).]. 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:22019001;
    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:NP515296.RAaHECyiTRluGWIrJ3vH5dRvWX2YqvXMdX7MostAVEVJk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:07+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" .
}