@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM
> .
@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:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_head
{
this:
np:hasAssertion
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_assertion
;
np:hasProvenance
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_assertion
a
np:Assertion
.
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_provenance
a
np:Provenance
.
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_assertion
{
miriam-gene:257194
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN01b0ff09158eedcc6e6bde2cf8533251
sio:SIO_000628
miriam-gene:257194
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_provenance
{
dgn-np:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_assertion
dcterms:description
"[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. 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:17052657
;
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:NP78439.RAHSGLXpra7BrMksrdUl_CHfnTuH7VQ2msA8gedeZ0DiM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:38+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" .
}