@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g
> .
@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:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_head
{
this:
np:hasAssertion
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_assertion
;
np:hasProvenance
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_assertion
a
np:Assertion
.
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_provenance
a
np:Provenance
.
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0751072
a
ncit:C7057
.
dgn-gda:DGN2a614fe67373e39dfd20e0982b6e72a0
sio:SIO_000628
miriam-gene:875
,
lld:C0751072
;
a
sio:SIO_001121
.
}
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_provenance
{
dgn-np:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_assertion
dcterms:description
"[Mutations in the microtubule associated protein tau (MAPT) and progranulin (PGRN) have been identified in several neurodegenerative disorders, such as frontotemporal lobar degeneration (FTLD), progressive supranuclear palsy (PSP), and corticobasal syndrome (CBS).]. 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:22818528
;
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:NP844118.RAT3sclS_56buEY_SWk-oC83oVyCDsObAbKrygZg43W6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:36+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" .
}