@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_head
{
this:
np:hasAssertion
dgn-np:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_assertion
;
np:hasProvenance
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
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{
miriam-gene:3606
a
ncit:C16612
.
lld:C0812393
a
ncit:C7057
.
dgn-gda:DGNb1690c764c57811e0f3c07d3ffed1fd3
sio:SIO_000628
miriam-gene:3606
,
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;
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.
}
dgn-np:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_provenance
{
dgn-np:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_assertion
dcterms:description
"[This study examined whether two promoter polymorphisms -137 G/C (rs187238) and -607 C/A (rs1946518) of IL-18 were associated with schizophrenia and six clinical symptoms (disorder of perception, thought disorder, disturbance of emotion, disorder of behavior and volition, suicide action, and aggressive action) to provide data for screening high-risk Han Chinese individuals.]. 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:21510800
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP509078.RAcvP-SqfWxzs1e6Jcb7rwgZ0uQDyhTm-50BlsOpR0dnU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:40+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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"v3.0.0" .
}