@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk
> .
@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:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_head
{
this:
np:hasAssertion
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_assertion
;
np:hasProvenance
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_provenance
;
np:hasPublicationInfo
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_assertion
a
np:Assertion
.
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_provenance
a
np:Provenance
.
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0391976
a
ncit:C7057
.
dgn-gda:DGN1aca9e93ec60b0c4e9b8a160437cb5c4
sio:SIO_000628
miriam-gene:1312
,
lld:C0391976
;
a
sio:SIO_001121
.
}
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_provenance
{
dgn-np:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_assertion
dcterms:description
"[Increased insight into how genetic variants within the COMT locus affect pain perception will contribute to improved understanding of the mechanisms involved in the development of common human pain disorders and may lead to improved strategies for 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:19374521
;
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:NP425516.RAr15tjElpyWqI51pvALOtDfpKmTKC7c3WFPIdwLw6ATk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}