@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w
> .
@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:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_head
{
this:
np:hasAssertion
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_assertion
;
np:hasProvenance
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_provenance
;
np:hasPublicationInfo
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_assertion
a
np:Assertion
.
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_provenance
a
np:Provenance
.
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_assertion
{
miriam-gene:9973
a
ncit:C16612
.
lld:C1839780
a
ncit:C7057
.
dgn-gda:DGN5793a44b8598c5ee23d5bf0dc39c50e8
sio:SIO_000628
miriam-gene:9973
,
lld:C1839780
;
a
sio:SIO_001121
.
}
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_provenance
{
dgn-np:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_assertion
dcterms:description
"[We recommend to include in the FXTAS testing guidelines both CCS hyperintensity and peripheral neuropathy and to consider them as new major radiologic and minor clinical criterion, respectively, for the diagnosis of FXTAS.]. 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:23077007
;
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:NP712881.RAmOk3bZksWDpFfSBG8fwXfWSuxVUvUzpg-4uqzGdon7w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}