@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc
> .
@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:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_head
{
this:
np:hasAssertion
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion
;
np:hasProvenance
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion
a
np:Assertion
.
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance
a
np:Provenance
.
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion
{
miriam-gene:4363
a
ncit:C16612
.
lld:C1864002
a
ncit:C7057
.
dgn-gda:DGN9ef635a61d110b4cafa14104c41ad5a6
sio:SIO_000628
miriam-gene:4363
,
lld:C1864002
;
a
sio:SIO_001122
.
}
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_provenance
{
dgn-np:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_assertion
dcterms:description
"[ The genotypic results observed show an ethnic difference in the frequencies of the MRP1 genetic polymorphisms between Japanese and Caucasians. Further studies are required to better understand the clinical consequences of the MRP1 genetic variants.]. 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:12856092
;
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:NP49764.RAReKLyZZL2OqnHM9g94Qz6o9JswHUVnbps18vCeQDoTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}