@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU
> .
@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:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_head
{
this:
np:hasAssertion
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion
;
np:hasProvenance
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_provenance
;
np:hasPublicationInfo
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion
a
np:Assertion
.
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_provenance
a
np:Provenance
.
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion
{
miriam-gene:121278
a
ncit:C16612
.
lld:C0233401
a
ncit:C7057
.
dgn-gda:DGN4e4ea9cdfca2fbd0c38cc388c1ebd52c
sio:SIO_000628
miriam-gene:121278
,
lld:C0233401
;
a
sio:SIO_001121
.
}
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_provenance
{
dgn-np:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_assertion
dcterms:description
"[The propensity of TPH2 to misfold upon oxidation of its cysteine residues is responsible for its catalytic lability and may be related to loss of serotonin neuronal function in PD and the emergence of non-motor (psychiatric) symptoms.]. 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:21105877
;
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:NP720149.RA5PI4UX33F8vclNrDHZQCX06hBGLvKdvJ2QCVSiCo3LU130_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" .
}