@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us
> .
@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:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_head
{
this:
np:hasAssertion
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_assertion
a
np:Assertion
.
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_provenance
a
np:Provenance
.
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:2896
a
ncit:C16612
.
lld:C0006012
a
ncit:C7057
.
dgn-gda:DGN5639c05969b992917ca4f05da6ee1e0e
sio:SIO_000628
miriam-gene:2896
,
lld:C0006012
;
a
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.
}
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_provenance
{
dgn-np:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_assertion
dcterms:description
"[Basing on the assumption that frontotemporal lobar degeneration (FTLD), schizophrenia and bipolar disorder (BPD) might share common aetiological mechanisms, we analyzed genetic variation in the FTLD risk gene progranulin (GRN) in a German population of patients with schizophrenia (nā=ā271) or BPD (nā=ā237) as compared with 574 age-, gender- and ethnicity-matched controls.]. 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:22505994
;
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:NP569195.RATREFQe9tLo0OItB9rZO3ytw2XZBatJ68NpFabjHU0Us130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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
<
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> , <
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" .
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}