@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs
> .
@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:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_head
{
this:
np:hasAssertion
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_assertion
;
np:hasProvenance
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_provenance
;
np:hasPublicationInfo
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_assertion
a
np:Assertion
.
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_provenance
a
np:Provenance
.
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_assertion
{
miriam-gene:405
a
ncit:C16612
.
lld:C0042133
a
ncit:C7057
.
dgn-gda:DGNbb37b0d793e5f3087b0dc0c197d4b2b8
sio:SIO_000628
miriam-gene:405
,
lld:C0042133
;
a
sio:SIO_001121
.
}
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_provenance
{
dgn-np:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_assertion
dcterms:description
"[In conclusion, the female reproductive tract expresses mRNA for the transcription factors AHR and ARNT, and changes in their expression at select target sites in specific pathological conditions such as endometriosis and uterine leiomyomas suggest a potential role for these factors in the pathogenesis of these conditions.]. 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:11756572
;
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:NP531558.RAnakDUYSvUfWoop5hQ0gwCzywjzY5zEvOHUdhtuId_Rs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}