@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o
> .
@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:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_head
{
this:
np:hasAssertion
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_assertion
;
np:hasProvenance
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_provenance
;
np:hasPublicationInfo
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_assertion
a
np:Assertion
.
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_provenance
a
np:Provenance
.
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN85bf7a7e9ca1892d340b6cd101f3291f
sio:SIO_000628
miriam-gene:4137
,
lld:C0497327
;
a
sio:SIO_001122
.
}
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_provenance
{
dgn-np:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_assertion
dcterms:description
"[In our familial FTD sample the estimation of TAU gene mutations accounted for a relative low prevalence (7.6%); based on our results we could argue the existence of other mutations in regulatory regions in the TAU gene or, on the other hand, other genes might be responsible for the most cases of familial FTD.]. 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:12565146
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61239.RA7EXpAx4iUc8s-Y5yFsg5LH_s5r_RfqoziyPXNK9l11o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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
<
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> , <
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
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"v2.1.0" .
}