@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag
> .
@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:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_head
{
this:
np:hasAssertion
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_assertion
;
np:hasProvenance
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_provenance
;
np:hasPublicationInfo
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_assertion
a
np:Assertion
.
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_provenance
a
np:Provenance
.
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_assertion
{
miriam-gene:4790
a
ncit:C16612
.
lld:C0270496
a
ncit:C7057
.
dgn-gda:DGN8ba4dba5a0240ef962db8d0900e01e7a
sio:SIO_000628
miriam-gene:4790
,
lld:C0270496
;
a
sio:SIO_001121
.
}
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_provenance
{
dgn-np:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_assertion
dcterms:description
"[A composite endophenotype of P50 ratio and frequency of leading saccades is consistent with the current clinical nosology of schizophrenia and bipolar disorder and parses patients with schizoaffective disorder, bipolar type, into two subgroups.]. 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:18056246
;
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:NP400958.RACwnQ4Jsz5f1v8VGx1u6JH1DO-pi4bTsNFHjQgBHN8ag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}