@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg
> .
@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:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_head
{
this:
np:hasAssertion
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion
;
np:hasProvenance
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance
;
np:hasPublicationInfo
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion
a
np:Assertion
.
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance
a
np:Provenance
.
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion
{
miriam-gene:1576
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN0cddb791e35c2de138f6d2e90543f864
sio:SIO_000628
miriam-gene:1576
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance
{
dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion
dcterms:description
"[To characterize pregnane X receptor (PXR) polymorphic variants in healthy Asian populations Chinese, Malay and Indian (n=100 each), and to investigate the association between PXR haplotypes and hepatic mRNA expression of PXR and its downstream target genes, CYP3A4 and ABCB1, as well as their influence on the clearance of doxorubicin in Asian breast cancer patients.]. 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:18981011
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}