@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg> .
@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:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_head {
  this: np:hasAssertion dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_assertion;
    np:hasProvenance dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_provenance;
    np:hasPublicationInfo dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_assertion a np:Assertion .
  
  dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_provenance a np:Provenance .
  
  dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_assertion {
  miriam-gene:554313 a ncit:C16612 .
  
  lld:C0175695 a ncit:C7057 .
  
  dgn-gda:DGN8faea8d04d0fe31515482ecca6a2f66f sio:SIO_000628 miriam-gene:554313, lld:C0175695;
    a sio:SIO_001121 .
}

dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_provenance {
  dgn-np:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_assertion dcterms:description
      "[To gain insight into the biochemical basis of Sotos syndrome, we tested the ability of each NSD1 PHD domain to bind histone H3 when methylated at regulatory sites Lys4, Lys9, Lys27, Lys36, and Lys79, and histone H4 at regulatory Lys20, and determined whether Sotos point mutations disrupted methylation site-specific binding.]. 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:21972110;
    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:NP930360.RAKDsrkcsefmvrytobd_ZtaGtx4eRUDaYrWd94FYAT5Mg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}