@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I
> .
@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:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_head
{
this:
np:hasAssertion
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_assertion
;
np:hasProvenance
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_provenance
;
np:hasPublicationInfo
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_assertion
a
np:Assertion
.
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_provenance
a
np:Provenance
.
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0016053
a
ncit:C7057
.
dgn-gda:DGNd81f6770e73ea51ccb2620809dc46213
sio:SIO_000628
miriam-gene:1312
,
lld:C0016053
;
a
sio:SIO_001122
.
}
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_provenance
{
dgn-np:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_assertion
dcterms:description
"[, COMT polymorphism is of potential pharmacological importance regarding individual differences in the metabolism of catechol drugs and may also be involved in the pathogenesis and treatment of FS through adrenergic mechanisms as well as genetic predisposition to FS.]. 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:12739038
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP89351.RAfOV92p0sE_yML6GqRwPTOHGBqcwQq6bdilqvxoqUU8I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}