@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_head
{
this:
np:hasAssertion
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion
;
np:hasProvenance
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance
;
np:hasPublicationInfo
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion
a
np:Assertion
.
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance
a
np:Provenance
.
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion
{
miriam-gene:3481
a
ncit:C16612
.
lld:C0175754
a
ncit:C7057
.
dgn-gda:DGN7c3368d603e6060907fdc2d196bf4773
sio:SIO_000628
miriam-gene:3481
,
lld:C0175754
;
a
sio:SIO_001121
.
}
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance
{
dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion
dcterms:description
"[Although ACC is extremely rare, recent advances in genomic and expression profiling, coupled with knowledge gained from the study of the inherited syndromes that increase ACC risk, are beginning to bring together a picture of a tumor type dependent on p53, the G2/M cell cycle transition and IGF2 stimulation.]. 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:19519204
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:22+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}