@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_head
{
this:
np:hasAssertion
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_assertion
;
np:hasProvenance
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_provenance
;
np:hasPublicationInfo
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_assertion
a
np:Assertion
.
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_provenance
a
np:Provenance
.
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_assertion
{
miriam-gene:2915
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN4fa4364de9d7f1ddc0c3e23bfb343967
sio:SIO_000628
miriam-gene:2915
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_provenance
{
dgn-np:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_assertion
dcterms:description
"[This excess can be corrected by reducing signaling by Gp1 mGluRs, and numerous studies have shown that inhibition of mGluR5, in particular, can ameliorate multiple mutant phenotypes in animal models of FXS.]. 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:21090964
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP853432.RAmxs4pxYjehSrrUF1npXl8v0Au6EU4251g5i2i3eMcms130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:11+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}