@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A
> .
@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:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_head
{
this:
np:hasAssertion
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_assertion
;
np:hasProvenance
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_provenance
;
np:hasPublicationInfo
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_assertion
a
np:Assertion
.
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_provenance
a
np:Provenance
.
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_assertion
{
miriam-gene:6790
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNfe213caa082bd8eba87485253268c273
sio:SIO_000628
miriam-gene:6790
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_provenance
{
dgn-np:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_assertion
dcterms:description
"[Amplification of AURKA has been detected at higher frequency in tumors from BRCA1 and BRCA2 mutation carriers than in sporadic breast tumors, suggesting that overexpression of AURKA and inactivation of BRCA1 and BRCA2 cooperate during tumor development and progression.]. 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:17627006
;
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:NP354936.RA5yPVxznkk_hiJzeL7mGXkUeYkkEI9gTQmt1QMBNFS6A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}