@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8
> .
@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:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_head
{
this:
np:hasAssertion
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_assertion
;
np:hasProvenance
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_provenance
;
np:hasPublicationInfo
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_assertion
a
np:Assertion
.
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_provenance
a
np:Provenance
.
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_assertion
{
miriam-gene:4842
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNa2a1c60305bce4534df235e2d0462b69
sio:SIO_000628
miriam-gene:4842
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_provenance
{
dgn-np:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_assertion
dcterms:description
"[To determine if NOS gene polymorphism affects the 5' flanking region that is immediately upstream of the transcription start site lying between the TATA element and CAATT boxes in PD, and differs significantly between patients with PD and normal controls, we studied genetic polymorphism in that region of the neuronal NOS gene in Chinese patients with PD living in Taiwan.]. 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:11809160
;
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:NP53871.RAAWpQFutPw8_D3GfMDaDaFEdPcHe4RSQrAbUxxGXCAx8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}