@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY
> .
@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:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_head
{
this:
np:hasAssertion
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_assertion
;
np:hasProvenance
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_assertion
a
np:Assertion
.
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_provenance
a
np:Provenance
.
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0241910
a
ncit:C7057
.
dgn-gda:DGNf7df65699a34f8d4eb21071c2bb717c1
sio:SIO_000628
miriam-gene:1557
,
lld:C0241910
;
a
sio:SIO_001121
.
}
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_provenance
{
dgn-np:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_assertion
dcterms:description
"[A polymorphic CYP2C19 gene was analyzed in 233 Japanese subjects, including 63 with Parkinson's disease, 92 with chronic liver diseases (35 chronic hepatitis, 19 liver cirrhosis, 16 hepatocellular carcinoma, 10 primary biliary cirrhosis and 12 autoimmune hepatitis), 14 with lung cancer (squamous cell carcinoma) and 64 healthy subjects to determine the genotype distributions of the CYP2C19 gene and to investigate its involvement in the diseases.]. 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:8890945
;
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:NP924489.RA13_ZUwFXk9x4kvjj8NVtxgAphEHQXqzOcsQV_IYnnoY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}