@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8
> .
@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:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_head
{
this:
np:hasAssertion
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_assertion
;
np:hasProvenance
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_provenance
;
np:hasPublicationInfo
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_assertion
a
np:Assertion
.
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_provenance
a
np:Provenance
.
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNe9271a5104b1f2dd79402a29f141157d
sio:SIO_000628
miriam-gene:4137
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_provenance
{
dgn-np:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_assertion
dcterms:description
"[The data presented here suggest that subhaplotypes of haplotype H1 may confer susceptibility to Parkinson's disease (PD), and that either allelic heterogeneity or different haplotype composition explain the divergent haplotype results.]. 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:17192721
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP130573.RAi-8YQgRGESvZQPSZY2YJuywZ0ACjUvJQpEFkYTwdoe8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:08+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" .
}