@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw
> .
@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:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_head
{
this:
np:hasAssertion
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_assertion
;
np:hasProvenance
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_assertion
a
np:Assertion
.
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_provenance
a
np:Provenance
.
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNe75ef4f921d1c132ad98836183f4a306
sio:SIO_000628
miriam-gene:2896
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_provenance
{
dgn-np:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_assertion
dcterms:description
"[Alterations in gene dosage have recently been associated with neurodegenerative disorders, such as Alzheimer's disease and Parkinson's disease, and deletions of the progranulin (PGRN) locus were recently described in patients with frontotemporal lobar degeneration (FTLD).]. 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:19940479
;
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:NP247414.RAFcKEhWuIThayfe4_o3DtNqHMh4QvBL8OGvr9oV4T8Yw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}