@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E
> .
@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/v4.0.0/void/
> .
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_head
{
this:
np:hasAssertion
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_assertion
;
np:hasProvenance
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_assertion
a
np:Assertion
.
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_provenance
a
np:Provenance
.
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_assertion
{
miriam-gene:23435
a
ncit:C16612
.
lld:C0236642
a
ncit:C7057
.
dgn-gda:DGNd65f0daa78b224b7cf3c005035f85a8a
sio:SIO_000628
miriam-gene:23435
,
lld:C0236642
;
a
sio:SIO_001121
.
}
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_provenance
{
dgn-np:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_assertion
dcterms:description
"[TARDBP mutation screening should be considered in familial frontotemporal dementia cases, even without signs or symptoms of motor neuron disease, especially when other more frequent causes of genetic frontotemporal dementia (i.e.]. 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:25853458
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1276516.RAuzDZ2oXARB_Q09iNALRuE1rnKGDIZJC5DEKlg3vWA8E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:24+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}