@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs
> .
@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:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_head
{
this:
np:hasAssertion
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_assertion
;
np:hasProvenance
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_provenance
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np:hasPublicationInfo
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_assertion
a
np:Assertion
.
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_provenance
a
np:Provenance
.
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN79663e380f4dd62080977614e38f020f
sio:SIO_000628
miriam-gene:4843
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_provenance
{
dgn-np:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_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: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:NP719528.RAP9cteujYysCAch7H9KDOSMzV8HqRqd4CQbBVUrOyQDs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}