@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo
> .
@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/v3.0.0/void/
> .
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_head
{
this:
np:hasAssertion
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_assertion
;
np:hasProvenance
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_provenance
;
np:hasPublicationInfo
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_assertion
a
np:Assertion
.
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_provenance
a
np:Provenance
.
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_assertion
{
miriam-gene:2005
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN00e7121d215951e2eed1f749a0718ade
sio:SIO_000628
miriam-gene:2005
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_provenance
{
dgn-np:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_assertion
dcterms:description
"[We here show for the first time that the most common genomic copy number gains in breast cancer, 1q21 and 1q32, are associated with overexpression of the ETS transcription factors ETV3 and ELF3 (but not ELK4) at these loci irrespective of molecular subtypes.]. 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:23329352
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP373429.RAjLC0iAPg9_VnPtE4ABNQRxenioy-CGH4mXynxKo-3fo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:15+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}