@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4
> .
@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:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_head
{
this:
np:hasAssertion
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_assertion
;
np:hasProvenance
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_assertion
a
np:Assertion
.
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_provenance
a
np:Provenance
.
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_assertion
{
miriam-gene:2017
a
ncit:C16612
.
lld:C0175754
a
ncit:C7057
.
dgn-gda:DGN5d12dafa1b3b2c634eae196567736a16
sio:SIO_000628
miriam-gene:2017
,
lld:C0175754
;
a
sio:SIO_001121
.
}
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_provenance
{
dgn-np:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_assertion
dcterms:description
"[Our results indicate that chromosome 11q13 amplification is uncommon in ACC, but that cyclin D1 and cortactin are frequently overexpressed and may therefore contribute to the growth and invasive potential of ACC.]. 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:17113340
;
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:NP346804.RApjsFYuzGQWo5ll3wi-XKzIcZTqqHV6SLn6omSvXiqh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}