@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0
> .
@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:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_head
{
this:
np:hasAssertion
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_assertion
;
np:hasProvenance
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_assertion
a
np:Assertion
.
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_provenance
a
np:Provenance
.
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0752347
a
ncit:C7057
.
dgn-gda:DGNba0708c87d76041bc4f5cf0792719672
sio:SIO_000628
miriam-gene:2896
,
lld:C0752347
;
a
sio:SIO_001121
.
}
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_provenance
{
dgn-np:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_assertion
dcterms:description
"[The recognition of the clinical phenotype associated with more than 50 different mutations in GRN has expanded the clinical knowledge of FTD to include presentations that resemble Alzheimer's disease, Lewy body disease, and corticobasal syndrome, with a variable age at onset (35-89 years) within families.]. 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:18771956
;
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:NP281630.RAc9cCoLJeKgRTIoP0i8jwORsbNpCStLfxZfEpiSAcgD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}