@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w
> .
@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:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_head
{
this:
np:hasAssertion
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_assertion
;
np:hasProvenance
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_assertion
a
np:Assertion
.
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_provenance
a
np:Provenance
.
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNec07f028fd4fd59820912a379974ce06
sio:SIO_000628
miriam-gene:2908
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_provenance
{
dgn-np:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_assertion
dcterms:description
"[The general lack of GR in adenocarcinomas contrasts with the high percentage of SCCs and HCCs expressing GR, and, along with the generation of chemoresistance by DEX, warrants prospective study of the effects of steroids on these 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:18269582
;
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:NP601113.RAEcfYRShXPfravq2NZA2xhs1IPwKKKtU9t38DtXaQE3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}