@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew
> .
@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:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_head
{
this:
np:hasAssertion
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_assertion
;
np:hasProvenance
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_provenance
;
np:hasPublicationInfo
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_assertion
a
np:Assertion
.
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_provenance
a
np:Provenance
.
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_assertion
{
miriam-gene:2643
a
ncit:C16612
.
lld:C0150055
a
ncit:C7057
.
dgn-gda:DGN51bb9142aa934f7fa027dd285e027816
sio:SIO_000628
miriam-gene:2643
,
lld:C0150055
;
a
sio:SIO_001121
.
}
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_provenance
{
dgn-np:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_assertion
dcterms:description
"[Recent advances in the genetics of pain and pain disorders include the discovery of the role of the sodium ion channel SCN9A in neuropathic pain as well as in inability to experience pain, and of GTP cyclohydrolase (GCH1) in setting the sensitivity to pain in normal individuals and modulating liability to chronic pain.]. 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:17508172
;
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:NP903482.RAqjbAcD6njQb6OXCW459MYqAT8IeBIROqZTi_Ibx9aew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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
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"v2.1.0" .
}