@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ
> .
@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/v3.0.0/void/
> .
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_head
{
this:
np:hasAssertion
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion
;
np:hasProvenance
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion
a
np:Assertion
.
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance
a
np:Provenance
.
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN1af24410605935cb7e3e2296fb1bbe98
sio:SIO_000628
miriam-gene:2896
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance
{
dgn-np:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion
dcterms:description
"[The discovery that mutations in the gene encoding for progranulin (GRN) cause frontotemporal lobar degeneration (FTLD) and other neurodegenerative diseases leading to dementia has brought renewed interest in progranulin and its functions in the central nervous system.]. 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:24018267
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}