@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg
> .
@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:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_head
{
this:
np:hasAssertion
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_assertion
;
np:hasProvenance
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_provenance
;
np:hasPublicationInfo
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_assertion
a
np:Assertion
.
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_provenance
a
np:Provenance
.
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_assertion
{
miriam-gene:1555
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN55e2480aa20542e1d731d68d962ec22e
sio:SIO_000628
miriam-gene:1555
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_provenance
{
dgn-np:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_assertion
dcterms:description
"[Molecular genetic studies of the cytochrome P450 system enzyme CYP2D6, which hydroxylates debrisoquine, have indicated an excess of mutant alleles in large series of patients with Parkinson's disease (PD) when compared with controls.]. 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:7651442
;
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:NP328001.RANNUdkx7p7u2HqqeAl6FBxgGyZTlh2X0W0rKkNebuGMg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:13+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" .
}