@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII
> .
@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:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_head
{
this:
np:hasAssertion
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_assertion
;
np:hasProvenance
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_provenance
;
np:hasPublicationInfo
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_assertion
a
np:Assertion
.
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_provenance
a
np:Provenance
.
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_assertion
{
miriam-gene:51008
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN4c546275b1028a09e486f1fc45b7d361
sio:SIO_000628
miriam-gene:51008
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_provenance
{
dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_assertion
dcterms:description
"[Eight Utah multigenerational families, each with three to six cases of schizophrenia, were phenotyped with two specific measures of inhibitory neurophysiological functioning, P50 auditory sensory gating (P50), and antisaccade ocular motor performance (AS).]. 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:10490714
;
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 .
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dgn-np:NP242702.RALQemNNRAvk9viR69PiHeWexLltrSVPapt5Qip3LLGII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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
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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
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"v2.1.0" .
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