@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk
> .
@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:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_head
{
this:
np:hasAssertion
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion
;
np:hasProvenance
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance
;
np:hasPublicationInfo
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion
a
np:Assertion
.
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance
a
np:Provenance
.
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion
{
miriam-gene:2004
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNf79946f8fdc74295aa7f532e43600794
sio:SIO_000628
miriam-gene:2004
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_provenance
{
dgn-np:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_assertion
dcterms:description
"[As the individual P3 latency of the majority of HD patients and all presymptomatic gene carriers was distributed within normal confidence intervals, and no correlation existed between ERP parameters and the signs of illness progression, the data appear to provide preliminary evidence against the valence of P3 in detecting the early cognitive impairment of HD.]. 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:15008503
;
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:NP713344.RA54ERjNss3RvqsuuMaAmncMsD8W4UT-n4dZ_UcbAcfwk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}