@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI
> .
@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:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_assertion
;
np:hasProvenance
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_assertion
a
np:Assertion
.
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_provenance
a
np:Provenance
.
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN6c8bb89004e5b38f8b6b62890197b14d
sio:SIO_000628
miriam-gene:4855
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_provenance
{
dgn-np:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_assertion
dcterms:description
"[Our results confirm that common risk factors in the major histocompatibility complex region and TCF4 gene are associated with schizophrenia in Han Chinese, but our results fail to show an association with SNP rs12807809 in the NRGN gene.]. 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:20673877
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53794.RACafNo1I-hWpKWxJB8xjh0Huy3pSW8Fjfywx8UgW-wnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}