@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4> .
@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:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_head {
   this: np:hasAssertion dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_assertion ;
    np:hasProvenance dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_provenance ;
    np:hasPublicationInfo dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_assertion a np:Assertion .
  dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_provenance a np:Provenance .
  dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_assertion {
   miriam-gene:219348 a ncit:C16612 .
  lld:C1832244 a ncit:C7057 .
  dgn-gda:DGN1b14b6672c039a66445d0006fc808491 sio:SIO_000628 miriam-gene:219348 , lld:C1832244 ;
    a sio:SIO_001121 .
}
dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_provenance {
   dgn-np:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_assertion dcterms:description "[This reduced the total number of candidate genes to 18 of which 17 (RAI17, PPIF, C10ORF56, SFTPA1, SFTPA2, SFTPA1B, SFTPA2B, SFTPD, C10ORF57, PLAC9, ANXA11, MAT1A, DYDC1, DYDC2, C10ORF58, TSPAN14 and SH2D4B) are shared with the CMD1C region.]. 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:18197198 ;
    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:NP396206.RAL737MJCLENL5wF6TdWbPQJeLLDoFVRt3WYdQlh46cf4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:55+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" .
}