@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI> .
@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:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_head {
  this: np:hasAssertion dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_assertion ;
    np:hasProvenance dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_provenance ;
    np:hasPublicationInfo dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_provenance a np:Provenance .
  dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_assertion {
  miriam-gene:118460 a ncit:C16612 .
  lld:C0041408 a ncit:C7057 .
  dgn-gda:DGNe737e4f2fb490cdca25e9f12a4c96855 sio:SIO_000628 miriam-gene:118460 , lld:C0041408 ;
    a sio:SIO_001121 .
}
dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_provenance {
  dgn-np:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_assertion dcterms:description "[We have used two single-copy Y chromosomal sequences specific for the short arm (47z and DP34) and one repeated sequence specific to the long arm (Y3.4) to study several patients with different types of sex chromosomal abnormalities, including three patients with gonadal dysgenesis and the karyotype 45,X/46,X + fragment, two females with Y autosomal translocations involving similar regions of the Y chromosome (46,XX,t(Y;14)(q11,p11) and 46,XY,t(Y;15)(q11,p11), two males with very small Y chromosomes (del(Y)(q12) and i(Yp], and a 45,X male with a small Y autosomal translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP427063.RA0q0TsdK_PW5QqSQSiwMzDRs75SyGunZ-ZCFJCE9nsAI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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> ;
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}