@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac
> .
@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:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_head
{
this:
np:hasAssertion
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_assertion
;
np:hasProvenance
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_provenance
;
np:hasPublicationInfo
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_assertion
a
np:Assertion
.
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_provenance
a
np:Provenance
.
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_assertion
{
miriam-gene:4988
a
ncit:C16612
.
lld:C0030201
a
ncit:C7057
.
dgn-gda:DGN0b4ba012f00da2e7890108da6def47fd
sio:SIO_000628
miriam-gene:4988
,
lld:C0030201
;
a
sio:SIO_001121
.
}
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_provenance
{
dgn-np:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_assertion
dcterms:description
"[Further studies are needed to fully investigate the effect of MOR A118G SNP on the post operative pain scores and SC values in the larger infant population in order to validate both the clinical significance of the skin conductance for routine pain assessment in infants and the observed genetic effect.]. 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:23046994
;
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:NP173698.RAOJJhaSOdbCHKuVPace-JMm69PpaYx6UlZ_EI6tZCKac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}