@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE
> .
@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:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_head
{
this:
np:hasAssertion
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_assertion
;
np:hasProvenance
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_provenance
;
np:hasPublicationInfo
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_assertion
a
np:Assertion
.
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_provenance
a
np:Provenance
.
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_assertion
{
miriam-gene:4968
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN0998129d2679b46665c942b062081208
sio:SIO_000628
miriam-gene:4968
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_provenance
{
dgn-np:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_assertion
dcterms:description
"[As OGG1 at chromosome band 3p25.3 overlaps a region exhibiting allelic imbalance (AI) in EOC, we also examined the frequency of AI of the OGG1 locus and its association with somatic mutations in the TP53 tumor suppressor gene, which is frequently mutated in EOC.]. 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:16211227
;
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:NP197001.RAjRqioBHlqWwzgSjLXAgDErtvAxA3mvgRQRyCZ-QkMtE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}