@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI
> .
@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:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_head
{
this:
np:hasAssertion
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_assertion
;
np:hasProvenance
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_provenance
;
np:hasPublicationInfo
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_assertion
a
np:Assertion
.
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_provenance
a
np:Provenance
.
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0010481
a
ncit:C7057
.
dgn-gda:DGNdcd8d6915c2fa6f1d607c86e7ed706ad
sio:SIO_000628
miriam-gene:7157
,
lld:C0010481
;
a
sio:SIO_001121
.
}
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_provenance
{
dgn-np:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_assertion
dcterms:description
"[The majority of benign adrenocortical tumors associated with CS are associated with defects of the cAMP signaling pathway, whereas adrenal cancer is linked to aberrant expression of growth factors and germline or somatic mutations of tumor suppressor genes such as TP53.]. 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:18493137
;
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:NP685805.RAC8N9serpG3G7Y4bEzvuHRXS-yOzsCWCZdyvagWUWGcI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}