@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI> .
@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:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_head {
  this: np:hasAssertion dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion;
    np:hasProvenance dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance;
    np:hasPublicationInfo dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion a np:Assertion .
  
  dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance a np:Provenance .
  
  dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion {
  miriam-gene:4153 a ncit:C16612 .
  
  lld:C0151526 a ncit:C7057 .
  
  dgn-gda:DGN70c8e6703e8de57097e07b5be1d3e16a sio:SIO_000628 miriam-gene:4153, lld:C0151526;
    a sio:SIO_001122 .
}

dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance {
  dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion dcterms:description
      "[Our data add to the knowledge about genetic predisposition to prematurity and suggest that the fetal MBL2 genotype might be an additional genetic factor contributing to the risk of premature delivery.]. 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:16912583;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}