@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s> .
@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 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:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_head {
  this: np:hasAssertion dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_assertion;
    np:hasProvenance dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_provenance;
    np:hasPublicationInfo dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_assertion a np:Assertion .
  
  dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_provenance a np:Provenance .
  
  dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_assertion {
  miriam-gene:2200 a ncit:C16612 .
  
  lld:C0011644 a ncit:C7057 .
  
  dgn-gda:DGNf1fa045c83ee457843bfb3a231b91af5 sio:SIO_000628 miriam-gene:2200, lld:C0011644;
    a sio:SIO_001122 .
}

dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_provenance {
  dgn-np:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_assertion dct:description
      "[ A 2-cM haplotype on chromosome 15q that contains FBN1 is associated with scleroderma in Choctaw Native Americans from Oklahoma. This haplotype may have been inherited from common founders about 10 generations ago and may contribute to the high prevalence of SSc that is now seen.]. 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:9778214;
    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:NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}