@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM
> .
@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:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_head
{
this:
np:hasAssertion
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_assertion
;
np:hasProvenance
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_provenance
;
np:hasPublicationInfo
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_assertion
a
np:Assertion
.
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_provenance
a
np:Provenance
.
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_assertion
{
miriam-gene:1022
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGNfa73f20f09f470cd00f3ed26442e9bd9
sio:SIO_000628
miriam-gene:1022
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_provenance
{
dgn-np:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_assertion
dcterms:description
"[Our study has demonstrated for the first time that the abnormal lower CD82 expression in ESCs induced by TCDD and estrogen may be an important molecular basis of endometriosis pathogenesis through enhancing the CCL2 secretion and CCR2 expression and the invasion of ESCs via MAPK and integrinβ1 signal pathway.]. 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:21685244
;
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:NP749673.RAy9xfVNerKMqmDVv_b8h4XIjtxtFrpYCV8je2z9GNykM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:34+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" .
}