@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_assertion
;
np:hasProvenance
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_provenance
;
np:hasPublicationInfo
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_assertion
a
np:Assertion
.
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_provenance
a
np:Provenance
.
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_assertion
{
miriam-gene:6335
a
ncit:C16612
.
lld:C0002768
a
ncit:C7057
.
dgn-gda:DGNca307754465a4149d63f01b60ebbd810
sio:SIO_000628
miriam-gene:6335
,
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.
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dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_provenance
{
dgn-np:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_assertion
dcterms:description
"[This study aimed to explore the role of a nonsynonymous single-nucleotide polymorphism, 3312G>T, in SCN9A, which was identified in probands with congenital indifference to pain, but which is also present in normal controls, in the prediction of individual baseline pain perception, and postoperative pain sensitivity in the general population.]. 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:23364568
;
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:NP608836.RAu2TtyHlpgRStgXi7x_7zL_Jf-dYX3FWxyX9L8HfUnOs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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
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> , <
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
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dgn-void:disgenetrdf
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}