@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q
> .
@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:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_head
{
this:
np:hasAssertion
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_assertion
;
np:hasProvenance
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_assertion
a
np:Assertion
.
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_provenance
a
np:Provenance
.
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_assertion
{
miriam-gene:8910
a
ncit:C16612
.
lld:C0233401
a
ncit:C7057
.
dgn-gda:DGN851e30bce64f5cddfff47e583263b708
sio:SIO_000628
miriam-gene:8910
,
lld:C0233401
;
a
sio:SIO_001121
.
}
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_provenance
{
dgn-np:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_assertion
dcterms:description
"[Herewith, this study may help to clarify whether neuropsychological and psychiatric symptoms are associated with the DYT11 mutation or are secondary to the burden of motor impairments that originated in early childhood.]. 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:22626943
;
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:NP850524.RAge4Ktz0Eg56uUlBT0x34ai3AiNlrqCTgl3fiYvI6S9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}