@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4
> .
@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:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_head
{
this:
np:hasAssertion
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_assertion
;
np:hasProvenance
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_provenance
;
np:hasPublicationInfo
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_assertion
a
np:Assertion
.
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_provenance
a
np:Provenance
.
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_assertion
{
miriam-gene:6908
a
ncit:C16612
.
lld:C0087012
a
ncit:C7057
.
dgn-gda:DGN83c82797f51bc296eaaec3b8ae22e682
sio:SIO_000628
miriam-gene:6908
,
lld:C0087012
;
a
sio:SIO_001122
.
}
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_provenance
{
dgn-np:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_assertion
dcterms:description
"[The low frequency of FXTAS in the studied material probably results from the fact that the syndrome is much more common in elderly persons (penetrance of the pathogenic premutation gene is higher among elderly individuals).]. 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:19235102
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP123432.RAL1oQ3_9Z1dMDOwjQEE3U3jgnEiOpfXEVpkBGned8Ln4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:49+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" .
}