@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII
> .
@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:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_head
{
this:
np:hasAssertion
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_assertion
;
np:hasProvenance
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_provenance
;
np:hasPublicationInfo
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_assertion
a
np:Assertion
.
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_provenance
a
np:Provenance
.
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN7683ae90c231f395b0b4264b11fbbeff
sio:SIO_000628
miriam-gene:57026
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_provenance
{
dgn-np:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_assertion
dcterms:description
"[We next compared cyclin D1 expression and the highest ranking CIN genes to a breast cancer expression database and discovered that expression of genes promoting CIN are highly enriched in luminal subtype and that high cyclin D1 and CIN expression correlate specifically in the luminal B subtype.]. 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:22538871
;
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:NP435785.RA8oFckE5j0QR06VAQRYOdxGG98hMrMvrCn94ncaH_EII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}