@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E
> .
@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#
> .
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_head
{
this:
np:hasAssertion
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_assertion
;
np:hasProvenance
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_assertion
a
np:Assertion
.
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_provenance
a
np:Provenance
.
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_assertion
{
miriam-gene:2033
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN1d5e0bf0472f1db2fdab4e2bfb279fe0
sio:SIO_000628
miriam-gene:2033
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_provenance
{
dgn-np:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_assertion
dcterms:description
"[Since statistical relationships between P300 components and both the COMT genetic polymorphism and schizophrenic disorders have been demonstrated, it seems reasonable to suggest that this COMT genetic variant may affect the P300 abnormality in 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:12566168
;
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:NP274854.RA3s12J561jXbiWNgd3S8M4ekxLljJZbUxTGcYuIDLY7E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}