@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs
> .
@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:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_head
{
this:
np:hasAssertion
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion
;
np:hasProvenance
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance
;
np:hasPublicationInfo
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion
a
np:Assertion
.
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance
a
np:Provenance
.
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0039494
a
ncit:C7057
.
dgn-gda:DGNb33a2025d5ab45a6aad24a9c4ade1937
sio:SIO_000628
miriam-gene:2099
,
lld:C0039494
;
a
sio:SIO_001121
.
}
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance
{
dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion
dcterms:description
"[The aim of this study is to identify any association between variants of the polymorphic estrogen receptor gene and various symptoms of temporomandibular disorder (TMD) including pain in the temporomandibular joint and masticatory muscles, joint crepitus, limited range of jaw movement, and bone changes in the condylar head.]. 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:20656393
;
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 .
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dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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
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"v2.1.0" .
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