@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s
> .
@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:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_head
{
this:
np:hasAssertion
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_assertion
;
np:hasProvenance
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_provenance
;
np:hasPublicationInfo
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_assertion
a
np:Assertion
.
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_provenance
a
np:Provenance
.
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_assertion
{
miriam-gene:196
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN10dbc7ea42e6f6d749d097cc8ab67bd9
sio:SIO_000628
miriam-gene:196
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_provenance
{
dgn-np:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_assertion
dcterms:description
"[Forced expression of NF1C suppressed the activity of the AHR promoter with C at rs10249788 stronger than that with T. Moreover, expression analysis of human uterine endometrial cancer (HEC) specimens showed greater upregulation of AHR and downregulation of NF1C than those of normal endometrium specimens.]. 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:23208493
;
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:NP424269.RAGp1S2iusP04f9ecEZ0TtbJMT4sBvDgRZTnK8FkUgB2s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}