@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs
> .
@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:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_head
{
this:
np:hasAssertion
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion
;
np:hasProvenance
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion
a
np:Assertion
.
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance
a
np:Provenance
.
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion
{
miriam-gene:8874
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNf4944d92ee7fd9f4c2f40be5802e0060
sio:SIO_000628
miriam-gene:8874
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance
{
dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion
dcterms:description
"[We recently suggested that, besides their origin in the ovary, reduction of CDC42 messenger RNA (a member of the RHO GTPase family) may contribute to explain why clear cell carcinomas are not uncommonly found limited to the ovary (stage I).]. 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:21944080
;
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:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}