@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4
> .
@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:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_head
{
this:
np:hasAssertion
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_assertion
;
np:hasProvenance
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_provenance
;
np:hasPublicationInfo
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_assertion
a
np:Assertion
.
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_provenance
a
np:Provenance
.
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0040822
a
ncit:C7057
.
dgn-gda:DGNd68b9aa55f2d392c207f9247f286c802
sio:SIO_000628
miriam-gene:1814
,
lld:C0040822
;
a
sio:SIO_001121
.
}
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_provenance
{
dgn-np:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_assertion
dcterms:description
"[These results suggest that DRD3 genotype and the variant DRD3Gly allelic variant is associated with the risk for and age at onset of ET, and with the risk for voice tremor, in Caucasian Spanish people.]. 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:19645064
;
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:NP685420.RAzH3K-FWZCchcK2iGdqGF0Of7_A87VPug9R5l-FmPet4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}