@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno
> .
@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:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_head
{
this:
np:hasAssertion
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_assertion
;
np:hasProvenance
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_provenance
;
np:hasPublicationInfo
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_assertion
a
np:Assertion
.
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_provenance
a
np:Provenance
.
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0033975
a
ncit:C7057
.
dgn-gda:DGN8b7f329371a588f1be81706830ee4b25
sio:SIO_000628
miriam-gene:1312
,
lld:C0033975
;
a
sio:SIO_001121
.
}
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_provenance
{
dgn-np:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_assertion
dcterms:description
"[The interplay between the catechol-O-methyltransferase (COMT) Val158Met polymorphism and environmental stress may have etiological relevance for psychosis, but differential effects have been reported in healthy control and patient groups, suggesting that COMT Val158Met interactions with stress may be conditional on background genetic risk for psychotic disorder.]. 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:21073668
;
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:NP184956.RAbDc-IRv4mzISIxK2ShSWpaF8OeY9ljjv9qZVKO6Ysno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}