@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo
> .
@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/v3.0.0/void/
> .
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_head
{
this:
np:hasAssertion
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_assertion
;
np:hasProvenance
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_provenance
;
np:hasPublicationInfo
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_assertion
a
np:Assertion
.
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_provenance
a
np:Provenance
.
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN4dbcb902441991b2ac7039087c516fa6
sio:SIO_000628
miriam-gene:1565
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_provenance
{
dgn-np:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_assertion
dcterms:description
"[Frequencies of both CYP2C9 and CYP2C19 allelic variants, as well as CYP2D6 detrimental alleles, in Italian subjects were similar to those of other Caucasian populations. Conversely, the prevalence of CYP2D6 gene duplication among Italians resulted very hi]. 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:15177309
;
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:NP77093.RAKHqU3galCPGrvYqSJKif1HiGGD18G6YTvWlfzapViyo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:22+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}