@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM
> .
@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:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_head
{
this:
np:hasAssertion
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_assertion
;
np:hasProvenance
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_assertion
a
np:Assertion
.
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_provenance
a
np:Provenance
.
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_assertion
{
miriam-gene:3309
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNf78ce0f63af2f4a570a21a31ef2360b8
sio:SIO_000628
miriam-gene:3309
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_provenance
{
dgn-np:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_assertion
dcterms:description
"[Genetic epidemiologic studies reveal that relatives of bipolar (BIP) probands are at increased risk for recurrent unipolar (RUP), BIP, and schizoaffective (SA) disorders, while relatives of schizophrenia (SZ) probands are at increased risk for SZ, SA, and RUP disorders.]. 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:10774477
;
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:NP919710.RAcVvtBvCZwh-Xcq-8HDiD47mbKIK_qoupP0nxjXjCDcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}