@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0
> .
@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:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_head
{
this:
np:hasAssertion
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_assertion
;
np:hasProvenance
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_assertion
a
np:Assertion
.
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_provenance
a
np:Provenance
.
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGN19a677ab04d23ff201703cc163487715
sio:SIO_000628
miriam-gene:5243
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_provenance
{
dgn-np:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_assertion
dcterms:description
"[The purpose of this study is to compare the genotype frequency of C3435T and G1199A polymorphisms in MDR1 between ESRD patients and healthy controls in the Chinese population to determine whether the alteration of the P-gp function is associated with ESRD.]. 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:17376299
;
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:NP334871.RAK6HpzK_unCzIJa7vPZrXnIKYooLTHCmIOWtHvEercW0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}