@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E
> .
@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:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_head
{
this:
np:hasAssertion
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_assertion
;
np:hasProvenance
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_assertion
a
np:Assertion
.
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_provenance
a
np:Provenance
.
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0010709
a
ncit:C7057
.
dgn-gda:DGN88d2fe55c3e3c86d9159829e468a156c
sio:SIO_000628
miriam-gene:5728
,
lld:C0010709
;
a
sio:SIO_001121
.
}
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_provenance
{
dgn-np:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_assertion
dcterms:description
"[These results show that reduced APC activity is sufficient to induce formation of epithelial inclusion cysts and support OEA development and suggest that induced HOXA10 expression and loss of PTEN are key mechanisms driving endometrioid histotype differentiation 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:23276799
;
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:NP597871.RAqRYB4Elur8BRxR1dYMvs-Tv1YVxKndVxsiJjIECWk0E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}