@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY
> .
@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:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_head
{
this:
np:hasAssertion
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_assertion
;
np:hasProvenance
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_provenance
;
np:hasPublicationInfo
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_assertion
a
np:Assertion
.
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_provenance
a
np:Provenance
.
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_assertion
{
miriam-gene:59348
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNbdefaa2ad1f98d21c5a71b4dbde51806
sio:SIO_000628
miriam-gene:59348
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_provenance
{
dgn-np:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_assertion
dcterms:description
"[Joint effect analyses indicated that all the variant genotypes of ZNF350 polymorphisms accounted for increased breast cancer risk among subjects carrying variant homozygote of BRCA1 rs799917, particularly for ZNF350 rs4986773 (OR = 2.03, 95%CI = 1.02-4.05, the test for gene-gene interaction P (int) = 0.059).]. 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:19484476
;
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:NP231840.RAyTAAzXVXr4_oijieKVudQzP1aLlggyZ7z9K_MpMJFWY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}