@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM
> .
@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:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_head
{
this:
np:hasAssertion
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_assertion
;
np:hasProvenance
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_provenance
;
np:hasPublicationInfo
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_assertion
a
np:Assertion
.
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_provenance
a
np:Provenance
.
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_assertion
{
miriam-gene:6697
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN6c9282061c2e5ddc44e1752b3ef37db6
sio:SIO_000628
miriam-gene:6697
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_provenance
{
dgn-np:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_assertion
dcterms:description
"[A linkage study in 122 European sibship families with five microsatellite and 17 single nucleotide polymorphism (SNP) markers in and around the SPR gene region, and an association analysis in 340 sporadic cases of Parkinson's disease and 680 control subjects from Germany with 40 SNPs.]. 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:16443856
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP66633.RA1foJgbv5RZLrMaojHd7cu24wLqLiV4cEuQKd_i2L0vM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}