@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE
> .
@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:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_head
{
this:
np:hasAssertion
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_assertion
;
np:hasProvenance
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_provenance
;
np:hasPublicationInfo
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_assertion
a
np:Assertion
.
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_provenance
a
np:Provenance
.
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_assertion
{
miriam-gene:3034
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNa9519e91c9b9c9edaa5f9ce06476b5c2
sio:SIO_000628
miriam-gene:3034
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_provenance
{
dgn-np:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_assertion
dcterms:description
"[The impact of genetic polymorphism of CYP1A2 that are related to the induction of the isozyme on the plasma levels of haloperidol (HAL) in 40 male smokers with schizophrenia was investigated.]. 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:11817502
;
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:NP488556.RA_luF4CT7mLmc32gHDbf5zrdjT17C6J5nb3S5yeqICrE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}