@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4> .
@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:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_head {
  this: np:hasAssertion dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion;
    np:hasProvenance dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance;
    np:hasPublicationInfo dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion a np:Assertion .
  
  dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance a np:Provenance .
  
  dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion {
  miriam-gene:3716 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
  dgn-gda:DGNd9efe629d53d4b475773fa40a90fc920 sio:SIO_000628 miriam-gene:3716, lld:C0085669;
    a sio:SIO_001121 .
}

dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance {
  dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion dcterms:description
      "[Although we isolated a mutation of JAK1 at residue Val658, which is found mutated in acute leukaemia patients, most of the mutations we identified are within the kinase domain and have yet to be identified in patients.]. 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:20868368;
    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:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:08+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" .
}