@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ
> .
@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:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_head
{
this:
np:hasAssertion
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_assertion
a
np:Assertion
.
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_provenance
a
np:Provenance
.
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_publicationInfo
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np:PublicationInfo
.
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dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_assertion
{
miriam-gene:7516
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN4968098e4cc8268d6a4d38045d39fbd1
sio:SIO_000628
miriam-gene:7516
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_provenance
{
dgn-np:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_assertion
dcterms:description
"[To test the hypothesis that polymorphisms in DSBs genes are associated with susceptibility to male infertility, we examined 11 single nucleotide polymorphisms in eight key DSBs genes (XRCC3, XRCC2, BRCA2, RAG1, XRCC5, LIG4, XRCC4 and ATM) in 580 infertility cases and 580 controls from a Chinese population-based case-control study (NJMU Infertility Study).]. 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:23630330
;
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:NP186456.RADBUtpYnNjibocv0wBwH2nGykpSc50E3QPgPjMtvEpCQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
}