@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw
> .
@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:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_head
{
this:
np:hasAssertion
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_assertion
;
np:hasProvenance
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_assertion
a
np:Assertion
.
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_provenance
a
np:Provenance
.
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN902e212011bc948f46d5fa38a602b613
sio:SIO_000628
miriam-gene:2896
,
lld:C0497327
;
a
sio:SIO_001122
.
}
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_provenance
{
dgn-np:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_assertion
dcterms:description
"[PGRN mutations at 17q21 may occur in apparently sporadic frontotemporal lobar dementia with ubiquitinated inclusions cases and in cases presenting with either primary progressive aphasia or the behavioral variant of frontotemporal dementia.]. 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:17522386
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP148839.RAbKxV_x1sJFsO01PkHBUP5WMwp3_jtxtOcfWXdagLHXw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:19+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" .
}