@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE
> .
@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:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_head
{
this:
np:hasAssertion
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_assertion
;
np:hasProvenance
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_provenance
;
np:hasPublicationInfo
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_assertion
a
np:Assertion
.
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_provenance
a
np:Provenance
.
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0175697
a
ncit:C7057
.
dgn-gda:DGNbfe10c7ad20fff5ff6c3ed7629f1229e
sio:SIO_000628
miriam-gene:1312
,
lld:C0175697
;
a
sio:SIO_001121
.
}
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_provenance
{
dgn-np:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_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-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:NP891134.RALQZqBAC9pNgLlGadne4LxvkEY_Ua95qEq4i-EatMdYE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}