@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU
> .
@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:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_assertion
;
np:hasProvenance
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_provenance
;
np:hasPublicationInfo
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_assertion
a
np:Assertion
.
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_provenance
a
np:Provenance
.
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN05b6d90ac1918b13a7459dc18618113f
sio:SIO_000628
miriam-gene:1813
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_provenance
{
dgn-np:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_assertion
dcterms:description
"[Results in SNPs previously reported as associated with schizophrenia were consistent with chance expectation, and four functional polymorphisms in COMT, DRD2, and HTR2A did not produce nominally significant evidence to support previous evidence for association.]. 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:18198266
;
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:NP157432.RAfLNYDc7fkpnqBk_LANdU0v08_gSjahT2k1vdW2hTbNU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}