@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8
> .
@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:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_head
{
this:
np:hasAssertion
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion
;
np:hasProvenance
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion
a
np:Assertion
.
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance
a
np:Provenance
.
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0030193
a
ncit:C7057
.
dgn-gda:DGNe1ed12b01fd326c1f2d29c7155834304
sio:SIO_000628
miriam-gene:1312
,
lld:C0030193
;
a
sio:SIO_001121
.
}
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_provenance
{
dgn-np:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_assertion
dcterms:description
"[Both human and mouse COMT genes possess functional polymorphisms contributing to interindividual variability in pain phenotypes such as sensitivity to noxious stimuli, severity of clinical pain, and response to pain treatment.]. 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:23701723
;
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:NP1080085.RAvohs9VgAz-FJjwcNVphXce_8tFGpDQX5loNRXDSFAk8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:55+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}