@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M
> .
@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:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_head
{
this:
np:hasAssertion
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_assertion
;
np:hasProvenance
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_provenance
;
np:hasPublicationInfo
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_assertion
a
np:Assertion
.
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_provenance
a
np:Provenance
.
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_assertion
{
miriam-gene:3481
a
ncit:C16612
.
lld:C0282160
a
ncit:C7057
.
dgn-gda:DGNa46e3116b52e147847f3c6e0411d681b
sio:SIO_000628
miriam-gene:3481
,
lld:C0282160
;
a
sio:SIO_001121
.
}
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_provenance
{
dgn-np:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_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-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:NP913759.RA1GeJ1u3Uo27m-rUACZLh-FMWQkMm6Ge3Eab1t_cba7M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}