@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo
> .
@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:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_head
{
this:
np:hasAssertion
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_assertion
;
np:hasProvenance
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_provenance
;
np:hasPublicationInfo
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_assertion
a
np:Assertion
.
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_provenance
a
np:Provenance
.
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_assertion
{
miriam-gene:29893
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN1f736e9bb8d33180bc727d3198617242
sio:SIO_000628
miriam-gene:29893
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_provenance
{
dgn-np:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_assertion
dcterms:description
"[In this study, using GT198 as a marker for microdissection, we find that ovarian tumor stromal cells harboring GT198 mutations are present in various types of ovarian cancer including high and low grade serous, endometrioid, mucinous, clear cell, and granulosa cell carcinomas and in precursor lesions such as inclusion cysts.]. 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:24097974
;
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:NP651693.RAjJRU3L5QrdBbhhd_bZbmSofAyQaQ_GjLjR4rq55RqTo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}