@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o
> .
@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:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_head
{
this:
np:hasAssertion
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_assertion
;
np:hasProvenance
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_provenance
;
np:hasPublicationInfo
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_assertion
a
np:Assertion
.
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_provenance
a
np:Provenance
.
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN1dfb58035b659169f49536dc7dc92ffb
sio:SIO_000628
miriam-gene:2896
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_provenance
{
dgn-np:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_assertion
dcterms:description
"[A recent study demonstrated that patients with frontotemporal dementia who presented with symptoms of schizophrenia show neuropathological findings consistent with GRN mutations, but were not tested for GRN mutations (Velakoulis, Walterfang, Mocellin, Pantelis, & McLean, 2009).]. 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:20087814
;
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:NP432293.RAaVcBDAdFVvuTiNcpswAo-hMf1uRVhYz4lb3G51Ak_4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}