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http://rdf.disgenet.org/nanopublications.trig#NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4
> .
@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:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_assertion
a
np:Assertion
.
dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_provenance
a
np:Provenance
.
dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_publicationInfo
a
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.
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{
miriam-gene:9567
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN4ee37185bcb804215059e4012603db28
sio:SIO_000628
miriam-gene:9567
,
lld:C0016667
;
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.
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dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_provenance
{
dgn-np:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_assertion
dcterms:description
"[The core aim of this review is to summarise two decades of molecular research leading to the characterisation of cellular and molecular pathways involved in the pathology of this disease and as a consequence to the identification of two new promising targets for rational therapy of fragile X syndrome, namely the group 1 metabotrope glutamate receptors (Gp1 mGluRs) and the gamma-amino butyric acid A receptors (GABA(A)Rs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19724010
;
prov:wasDerivedFrom
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;
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:NP295637.RAtHJS1VWESbv3eVoCBraqWdDS2wSRvPks-ykpkU8vcc4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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
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<
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> , <
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> , <
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
> ;
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