@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_assertion
a
np:Assertion
.
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_provenance
a
np:Provenance
.
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:57532
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN1b3f311d91913fa2aacf40321e7b4fee
sio:SIO_000628
miriam-gene:57532
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_provenance
{
dgn-np:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_assertion
dcterms:description
"[The purpose of this chapter is to discuss the role of the fragile X mental retardation protein (FMRP) in the spinal sensory system and the potential for use of the mouse model of fragile X syndrome to better understand some aspects of the human syndrome as well as advance knowledge in other areas of investigation, such as pain amplification, an important aspect of clinical pain disorders.]. 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:22009347
;
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:NP931950.RAwxk2fFDjXnTvE9TVQU9pugocaaG9nzmhHoU-HWUA43g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:47+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
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;
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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"v4.0.0" .
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