@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8
> .
@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:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_head
{
this:
np:hasAssertion
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_assertion
;
np:hasProvenance
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_provenance
;
np:hasPublicationInfo
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_assertion
a
np:Assertion
.
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_provenance
a
np:Provenance
.
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGN881fb9f27d095f5a24326cf475483431
sio:SIO_000628
miriam-gene:6531
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_provenance
{
dgn-np:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_assertion
dcterms:description
"[Striatal DAT binding was decreased not only in the control subjects with 44 or 43 repeats, but in ones with 42 repeats, suggesting that an expansion as low as 42 repeats might constitute a susceptibility gene for parkinsonism.]. 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:19380697
;
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:NP445530.RALIByzxsk6bCAfQxH_GXrMfvrxn7KO8naLbOviXIuJL8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}