@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A> .
@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:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_head {
  this: np:hasAssertion dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_assertion;
    np:hasProvenance dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_provenance;
    np:hasPublicationInfo dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_assertion a np:Assertion .
  
  dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_provenance a np:Provenance .
  
  dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_assertion {
  miriam-gene:914 a ncit:C16612 .
  
  lld:C1868674 a ncit:C7057 .
  
  dgn-gda:DGNe406cd1a178ad504ebdac3fae66eb148 sio:SIO_000628 miriam-gene:914, lld:C1868674;
    a sio:SIO_001121 .
}

dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_provenance {
  dgn-np:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_assertion dcterms:description
      "[The gene defective in X-linked lymphoproliferative disease, SH2D1A (also named SAP or DSHP), has been identified and shown to code for an adapter protein that interacts with signaling lymphocytic activation molecule (SLAM) and several other members of the CD2 superfamily.]. 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:12629654;
    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:NP389742.RA1vqHZu8AxcNDkc-YL1cY6nLRQaznV_EPS2NsoNn-R_A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}