@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U
> .
@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:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_head
{
this:
np:hasAssertion
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_assertion
;
np:hasProvenance
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_provenance
;
np:hasPublicationInfo
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_assertion
a
np:Assertion
.
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_provenance
a
np:Provenance
.
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN88cbabba570233ac2afbab80cb6f5628
sio:SIO_000628
miriam-gene:4524
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_provenance
{
dgn-np:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_assertion
dcterms:description
"[In a prospective, population-based cohort study among 5,920 participants aged 55 years or older, we observed that the TT variant of the methylenetetrahydrofolate reductase C677T polymorphism is associated with an increased risk for Parkinson's disease in smokers.]. 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:15929053
;
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:NP723359.RAh_6u3WUyZvRg7B2khdxWmpBs7kBQGCy2iX2VfAAJI7U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}