@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU
> .
@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:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_head
{
this:
np:hasAssertion
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_assertion
;
np:hasProvenance
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_assertion
a
np:Assertion
.
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_provenance
a
np:Provenance
.
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN6a5bff2bf0f050d31f90bd90dbb7cd41
sio:SIO_000628
miriam-gene:3342
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_provenance
{
dgn-np:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_assertion
dcterms:description
"[Recurrence rate in patients with epithelial ovarian cancer is seemingly associated with specific genetic alterations detected by CGH, but the specific genes involved and the implications of these findings await further studies.]. 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:19380021
;
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:NP491952.RAHOJMJCW7ELiQe6ZE6KKzs9jRI_HNRGQNnQR--jVuOvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}