@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU
> .
@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:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_head
{
this:
np:hasAssertion
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion
;
np:hasProvenance
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion
a
np:Assertion
.
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance
a
np:Provenance
.
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0001624
a
ncit:C7057
.
dgn-gda:DGNb0ced9e5564fc7524512b0dde45d40c9
sio:SIO_000628
miriam-gene:7157
,
lld:C0001624
;
a
sio:SIO_001121
.
}
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_provenance
{
dgn-np:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_assertion
dcterms:description
"[As p53 protein is a regulator of guanine nucleotide synthesis, the loss of normal inhibitory regulation by the p53 mutation would serve to increase the availability of GTP for the transduction of signals essential for increased cell growth and hormone expression in the adrenal tumors.]. 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:8106638
;
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:NP343298.RA2bEqsRb5WXHqD8EkGNuqz-QFdvpIOYmAi8h6fDYJSuU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}