@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion
;
np:hasProvenance
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance
;
np:hasPublicationInfo
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion
a
np:Assertion
.
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance
a
np:Provenance
.
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion
{
miriam-gene:2932
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN74e84ab2addadb315d7faf3e46c34117
sio:SIO_000628
miriam-gene:2932
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance
{
dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion
dcterms:description
"[By using the Molecular Genetics of Schizophrenia data set, we were able to test and confirm that markers in NRXN1 and GSK3B have epistatic interactions in human populations that can jointly modulate risk of schizophrenia.]. 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:22832527
;
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:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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
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"v2.1.0" .
}