@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y
> .
@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:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_head
{
this:
np:hasAssertion
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_assertion
;
np:hasProvenance
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_assertion
a
np:Assertion
.
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_provenance
a
np:Provenance
.
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0006111
a
ncit:C7057
.
dgn-gda:DGN98960b0afe01ce72d12d1062bccd939d
sio:SIO_000628
miriam-gene:2896
,
lld:C0006111
;
a
sio:SIO_001121
.
}
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_provenance
{
dgn-np:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_assertion
dcterms:description
"[Due to the functions of PGRN in neuronal survival and the clinicopathological overlaps between FTD and other dementias it is likely that reduced PGRN expression is associated with the progression of other neurodegenerative brain diseases including Alzheimer's disease.]. 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:17168647
;
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:NP720821.RAY8BC9AVCtxkFuP487XbVCOKe6PkLUPB7TmSvAAJEQ3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}