@prefix semsc: <
http://semanticscience.org/resource/
> .
@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@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 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:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_head
{
this:
np:hasAssertion
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion
;
np:hasProvenance
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance
;
np:hasPublicationInfo
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion
a
np:Assertion
.
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance
a
np:Provenance
.
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion
{
miriam-gene:91752
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN0f723557588e1d583221557c2a14a844
semsc:SIO_000628
miriam-gene:91752
,
lld:C0036341
;
a
semsc:SIO_001121
.
}
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_provenance
{
dgn-np:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_assertion
dct:description
"[The allelic association at the ZNF804A locus is now one of the most compelling in schizophrenia to date, and supports the accumulating data suggesting overlapping genetic risk between schizophrenia and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
semsc:SIO_000772
miriam-pubmed:20368704
;
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:NP207310.RADfcJCiC1_JVb48GhVDqlTviJ7rrsqq65_r9s_Fgv_14130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:54+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
semsc:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}