@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg
> .
@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:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_head
{
this:
np:hasAssertion
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion
;
np:hasProvenance
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance
;
np:hasPublicationInfo
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion
a
np:Assertion
.
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance
a
np:Provenance
.
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion
{
miriam-gene:1559
a
ncit:C16612
.
lld:C0013182
a
ncit:C7057
.
dgn-gda:DGN0cb37ec5625e9a0de8b20425cdbb0886
sio:SIO_000628
miriam-gene:1559
,
lld:C0013182
;
a
sio:SIO_001122
.
}
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance
{
dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion
dcterms:description
"[This group of Inuit individuals are the first population in which no 2C9*2 or *3 alleles have been detected so far. Therefore, these alleles may be extremely rare or absent, and unless other novel polymorphisms exist in this Inuit group one would not anticipate any CYP2C9 poor metabolizer subjects among this population.]. 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:11697742
;
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:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}