@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk
> .
@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:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_head
{
this:
np:hasAssertion
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion
;
np:hasProvenance
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance
;
np:hasPublicationInfo
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion
a
np:Assertion
.
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance
a
np:Provenance
.
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN682562c2c254bb8f12cf367e860c078f
sio:SIO_000628
miriam-gene:4137
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_provenance
{
dgn-np:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_assertion
dcterms:description
"[Frontotemporal dementia is commonly associated with parkinsonism in several sporadic (i.e., progressive supranuclear palsy, corticobasal degeneration) and familial neurodegenerative disorders (i.e., frontotemporal dementia associated with parkinsonism and MAPT or progranulin mutations in chromosome 17).]. 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:21892619
;
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:NP280498.RAAMw2fJdNbMupu4_ZXQxzKs_sePH1iqDPml0-7oRJ7Gk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}