@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4
> .
@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:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_head
{
this:
np:hasAssertion
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_assertion
;
np:hasProvenance
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_assertion
a
np:Assertion
.
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_provenance
a
np:Provenance
.
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_assertion
{
miriam-gene:3176
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN74ce7fc283db78ad51ac6db3db5d6782
sio:SIO_000628
miriam-gene:3176
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_provenance
{
dgn-np:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_assertion
dcterms:description
"[These results, combined with previous findings indicating alterations in the frequency for the HNMT Thr105Ile polymorphism in patients with PD, suggest that alterations of histamine homeostasis in the SNC are associated with the risk of movement disorders.]. 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:18543121
;
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:NP731117.RAY9JTQXA6F455w1G74SxIDO-JKW7Q7t8j60hAFGsfhF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}