@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY
> .
@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/v3.0.0/void/
> .
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_head
{
this:
np:hasAssertion
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_assertion
;
np:hasProvenance
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_assertion
a
np:Assertion
.
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_provenance
a
np:Provenance
.
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C2931498
a
ncit:C7057
.
dgn-gda:DGNdc15989989f63d0a6a9e5e65429fd4a7
sio:SIO_000628
miriam-gene:2332
,
lld:C2931498
;
a
sio:SIO_001121
.
}
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_provenance
{
dgn-np:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_assertion
dcterms:description
"[This finding is in agreement with the hypothesis that the incidence of intermediate FMR1 alleles in MRX populations does not seem to be higher than in control populations, and it emphasizes the importance of FMRP detection as a diagnostic tool for fragile X syndrome.]. 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:11030419
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP409124.RAqKLK-lCNMoO2ppmwEpmcdFOR7MsQUuenO0Eqz2edEwY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:38+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}