@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA> .
@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:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_head {
  this: np:hasAssertion dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_assertion;
    np:hasProvenance dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_provenance;
    np:hasPublicationInfo dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_assertion a np:Assertion .
  
  dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_provenance a np:Provenance .
  
  dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_assertion {
  miriam-gene:7124 a ncit:C16612 .
  
  lld:C0162359 a ncit:C7057 .
  
  dgn-gda:DGNfe810ac584258b71f28227bd2565f73d sio:SIO_000628 miriam-gene:7124, lld:C0162359;
    a sio:SIO_001121 .
}

dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_provenance {
  dgn-np:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_assertion dcterms:description
      "[Furthermore, by exploring systematic 3D conformation analysis and calculation of residue relative solvent accessibility (RSA) for all the reported mutated amino acid sites on EDA's TNF homology domain, we found that the site mutations at the interior may be linked to XLHED, while those at the surface are more likely to be associated with NSH.]. 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:23625373;
    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:NP805044.RA43OLNDSiqMoZVsyBL8qgg4phpniJAL7QnrPtTTR4RzA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:13+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" .
}