@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE
> .
@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#
> .
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_head
{
this:
np:hasAssertion
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion
;
np:hasProvenance
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance
;
np:hasPublicationInfo
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion
a
np:Assertion
.
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance
a
np:Provenance
.
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion
{
miriam-gene:2477
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGN9ff669e943a2210d6deaf65208bb5396
sio:SIO_000628
miriam-gene:2477
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance
{
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion
dcterms:description
"[Special emphasis has been placed on the possibility that the modest elevation of 'toxic' FMR1 mRNA in the carriers of grey zone alleles may present an additional risk for some neurodegenerative diseases, such as those associated with parkinsonism, by synergizing with either other susceptibility genes or environmental poisons.]. 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:23560306
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
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 .
}
dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}