@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI
> .
@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:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_head
{
this:
np:hasAssertion
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_assertion
;
np:hasProvenance
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_provenance
;
np:hasPublicationInfo
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_assertion
a
np:Assertion
.
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_provenance
a
np:Provenance
.
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0040517
a
ncit:C7057
.
dgn-gda:DGNbcb602a96d4c71078c4e93bc1c7693bc
sio:SIO_000628
miriam-gene:1437
,
lld:C0040517
;
a
sio:SIO_001121
.
}
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_provenance
{
dgn-np:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_assertion
dcterms:description
"[The most robust metabolic findings are the lowered CSF HVA in many TS patients, and the positive response of symptoms to dopamine blockers and clonidine particularly, which would be consistent with dopamine receptor hypersensitivity and possible noradrenergic-dopaminergic interactions in TS.]. 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:6324164
;
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:NP487433.RAgdbx9J1ES6MgGtGdDUuwBJa5tnBeOwPMOzD3ZS5h2fI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}