@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU
> .
@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:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_head
{
this:
np:hasAssertion
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion
;
np:hasProvenance
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion
a
np:Assertion
.
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance
a
np:Provenance
.
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0030193
a
ncit:C7057
.
dgn-gda:DGNf6e4cd8eec1905cba205e0925c9667b0
sio:SIO_000628
miriam-gene:1312
,
lld:C0030193
;
a
sio:SIO_001122
.
}
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_provenance
{
dgn-np:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_assertion
dcterms:description
"[This study suggests that genetic variability in the COMT gene influence the efficacy of morphine in cancer patients with pain, and that increased understanding of this variability is reached by expanding from analyses of single SNPs to haplotype construct]. 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:19094200
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP136993.RAuTi4hv9zi2U0ioE2F4xORII27fsTkymOYU5xm706DfU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:49+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" .
}