@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I
> .
@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:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_head
{
this:
np:hasAssertion
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_assertion
;
np:hasProvenance
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_provenance
;
np:hasPublicationInfo
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_assertion
a
np:Assertion
.
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_provenance
a
np:Provenance
.
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_assertion
{
miriam-gene:497258
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN28002c27a36773d834130dcab088d1d8
sio:SIO_000628
miriam-gene:497258
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_provenance
{
dgn-np:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_assertion
dcterms:description
"[After reviewing the available studies on the influence of genotype on brain volume in schizophrenia, it is evident that the BDNF and COMT genes are clearly favourites for genetic imaging studies.]. 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:18332664
;
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:NP312631.RAASITPnTC5zGA9NyhpzOPlDyVkcWtgieZ3_ufMHXx2_I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}