@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0
> .
@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:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_head
{
this:
np:hasAssertion
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_assertion
;
np:hasProvenance
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_provenance
;
np:hasPublicationInfo
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_assertion
a
np:Assertion
.
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_provenance
a
np:Provenance
.
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0030193
a
ncit:C7057
.
dgn-gda:DGN46889e3be6fc80d03b410446b7f20ad2
sio:SIO_000628
miriam-gene:1312
,
lld:C0030193
;
a
sio:SIO_001122
.
}
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_provenance
{
dgn-np:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_assertion
dcterms:description
"[Three common haplotypes of the human COMT gene, divergent in two synonymous and one nonsynonymous (val(158)met) position, designated as low (LPS), average (APS), and high pain sensitive (HPS), are associated with experimental pain sensitivity and risk of developing chronic musculoskeletal pain conditions.]. 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:19365560
;
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:NP732269.RApvZE0aDsBTfPP9PLbK1_JcKFUwYLMldIrjihPx40-M0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:17+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" .
}