@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc
> .
@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:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_head
{
this:
np:hasAssertion
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_assertion
;
np:hasProvenance
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_provenance
;
np:hasPublicationInfo
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_assertion
a
np:Assertion
.
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_provenance
a
np:Provenance
.
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0007859
a
ncit:C7057
.
dgn-gda:DGN326bffa0c66b1a4e01aee31ea0d07e43
sio:SIO_000628
miriam-gene:1312
,
lld:C0007859
;
a
sio:SIO_001121
.
}
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_provenance
{
dgn-np:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_assertion
dcterms:description
"[Genetic variations in the catechol-O-methyltransferase (COMT) gene have been associated with experimental pain and risk of chronic pain development, but no studies have examined genetic predictors of neck pain intensity and other patient characteristics after motor vehicle collision (MVC).]. 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:20688576
;
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:NP324665.RAY5P09QyhhwWHQrwoRpxPknu_gCl5c8f6hDuSURx61gc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}