@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo
> .
@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:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_head
{
this:
np:hasAssertion
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_assertion
;
np:hasProvenance
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_provenance
;
np:hasPublicationInfo
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_assertion
a
np:Assertion
.
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_provenance
a
np:Provenance
.
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN25229a1130c0c534e02a114f8ed0fc58
sio:SIO_000628
miriam-gene:8170
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_provenance
{
dgn-np:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_assertion
dcterms:description
"[The XRCC3 a4541g polymorphism, situated in the 5'UTR, and the intronic XRCC3 a17893g polymorphism were not associated with EOC risk in general, but when the serous EOC subset only was analysed, the OR for heterozygotes for a4541g was 1.0 (0.9-1.2) and for the rare homozygotes 0.5 (0.3-0.9).]. 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:15924337
;
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:NP363794.RAb4kJVK63BYPCiMGS2PHupnIEmWd7Cp1r7kpfz0rvOmo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}