@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g> .
@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:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_head {
  this: np:hasAssertion dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_assertion;
    np:hasProvenance dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_provenance;
    np:hasPublicationInfo dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_assertion a np:Assertion .
  
  dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_provenance a np:Provenance .
  
  dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0042974 a ncit:C7057 .
  
  dgn-gda:DGN8bebe8cfb561fb8a6fa01989ae4671b2 sio:SIO_000628 miriam-gene:7450, lld:C0042974;
    a sio:SIO_001122 .
}

dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_provenance {
  dgn-np:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_assertion dcterms:description
      "[We used human rADAMTS-13-WT to digest 11 full-length recombinant forms of VWF carrying molecular abnormalities identified in patients with VWD type 2A (E1638K and P1648S), type 2B (InsM1303, R1306W, R1308P and V1314F) and type 2M (G1324A, E1359K, K1362T, R1374H and I1425F).]. 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:17087728;
    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:NP577999.RAM6qiLDnAXqqVhbmpqG9a6hiUeqnWNqdfl0JroEfp94g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:07+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: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" .
}