@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_head {
  this: np:hasAssertion dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion;
    np:hasProvenance dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance;
    np:hasPublicationInfo dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion a np:Assertion .
  
  dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance a np:Provenance .
  
  dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGNf4ef335efb2cb6af154e67a2e1a33fd5 sio:SIO_000628 miriam-gene:324, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance {
  dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion dcterms:description
      "[In addition to polymorphic analysis, we have also searched germline mutations of the APC gene in eight individuals (26 percent of all 31 at risk persons) of another two FAP families which could not be diagnosed definitely by linkage analysis.]. 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:7913010;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:47+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}