@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik
> .
@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:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_head
{
this:
np:hasAssertion
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion
;
np:hasProvenance
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance
;
np:hasPublicationInfo
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion
a
np:Assertion
.
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance
a
np:Provenance
.
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0085084
a
ncit:C7057
.
dgn-gda:DGN554893134212ea29f708759776c49222
sio:SIO_000628
miriam-gene:4137
,
lld:C0085084
;
a
sio:SIO_001121
.
}
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_provenance
{
dgn-np:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_assertion
dcterms:description
"[Two hundred and twenty-three consecutive patients fulfilling clinical diagnostic criteria for frontotemporal lobar degeneration (FTLD), and 259 patients with motor neuron disease (MND), for whom genomic DNA was available, were investigated for the presence of mutations in tau (MAPT) and progranulin (PGRN) genes.]. 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:18192287
;
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:NP801761.RAKPmTB9-SoSRqLYhaQVv00FNT4jOX1O06gBhEfUdrNik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}