@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_head
{
this:
np:hasAssertion
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_assertion
;
np:hasProvenance
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_provenance
;
np:hasPublicationInfo
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_assertion
a
np:Assertion
.
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_provenance
a
np:Provenance
.
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_assertion
{
miriam-gene:1573
a
ncit:C16612
.
lld:C0041671
a
ncit:C7057
.
dgn-gda:DGNeb018553c261a88a82b6017674fbf9e1
sio:SIO_000628
miriam-gene:1573
,
lld:C0041671
;
a
sio:SIO_001122
.
}
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_provenance
{
dgn-np:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_assertion
dcterms:description
"[ The CYP2J2*7 variant represents a relatively rare polymorphism in Chinese, with the allele frequency being comparable to that of Korean, but significantly lower than those of African and White groups. This data may be informative to design population-bas]. 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:16182271
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP95942.RANA6SpMHlgH8N2TVReAxPS0mtpAH1kZlysWH683BY_bg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}