@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s
> .
@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/v4.0.0/void/
> .
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_head
{
this:
np:hasAssertion
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_assertion
a
np:Assertion
.
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_provenance
a
np:Provenance
.
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNd8af5f8adaa00924974648e93164f9a8
sio:SIO_000628
miriam-gene:1312
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_provenance
{
dgn-np:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_assertion
dcterms:description
"[The identification of a gentic marker associated with significant alterations in enzyme activity will facilitate the analysis of a possible role for the COMT gene in neuropsychiatric conditions in which abnormalities in catecholamine neurotransmission are believed to occur, including mood disorders, schizophrenia, obsessive compulsive disorder, alcohol and substance abuse, and attention deficit hyperactivity 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:8807664
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1357460.RACmWCkn5IMs21VFQcq0FuXBxfNel-NUYQOWAlLswTB9s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:01+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}