@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY
> .
@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:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_head
{
this:
np:hasAssertion
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_assertion
;
np:hasProvenance
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_assertion
a
np:Assertion
.
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_provenance
a
np:Provenance
.
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGNcbc06506137cc39e3854f28ad0f66201
sio:SIO_000628
miriam-gene:2332
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_provenance
{
dgn-np:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_assertion
dcterms:description
"[Because of the high prevalence of FMR1 premutation in the general population, the description and characterization of the FXTAS syndrome is of great interest as it may represent one of the more common monogenic causes of ataxia, tremor, and dementia.]. 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:17917121
;
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:NP633759.RA7ed57rSN8H8mke2G5vypQrh9ty5DyS8XWacjbfvmZqY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:32+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" .
}