@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg
> .
@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:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_head
{
this:
np:hasAssertion
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_assertion
;
np:hasProvenance
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_assertion
a
np:Assertion
.
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_provenance
a
np:Provenance
.
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_assertion
{
miriam-gene:1577
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGNe9315bdb981920a754a2f2a2f6f67570
sio:SIO_000628
miriam-gene:1577
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_provenance
{
dgn-np:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_assertion
dcterms:description
"[We found significantly lower levels of CYP1B1 and CYP3A7, higher levels of SULT2B1, UGT2B7 and GSTP1, and no differences in expression of COMT, CYP1A1, CYP3A5, SULT1E1 and SULT2A1 in the endometrial cancers.]. 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:20887769
;
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:NP727172.RACHyaEja06YYr8K8bAV_EkGanHjx9uQ5oN_R-raeUYHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}