@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_head
{
this:
np:hasAssertion
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_assertion
;
np:hasProvenance
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_assertion
a
np:Assertion
.
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_provenance
a
np:Provenance
.
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_assertion
{
miriam-gene:5591
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN009c93b07c19cfb868176a3a59466ead
sio:SIO_000628
miriam-gene:5591
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_provenance
{
dgn-np:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_assertion
dcterms:description
"[Because single nucleotide polymorphisms (SNPs) are the most subtle genetic variation in the genome, to examine these hypotheses, we have genotyped 30 SNPs in all five NHEJ genes (Ku70, Ku80, DNA-PKcs, Ligase IV, and XRCC4) in 254 primary breast cancer patients and 379 healthy controls.]. 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:12750264
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP65930.RAE4-HWZmJ4QQWjBiW5nWz_BS-pRGzKwxYbm4vOqn2NtI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:16+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}