@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA
> .
@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:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_head
{
this:
np:hasAssertion
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion
;
np:hasProvenance
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion
a
np:Assertion
.
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance
a
np:Provenance
.
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN82ad4dc076a9d3080da90d1e5346e0ae
sio:SIO_000628
miriam-gene:1312
,
lld:C0004936
;
a
sio:SIO_001121
.
}
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_provenance
{
dgn-np:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_assertion
dcterms:description
"[Future longitudinal studies focusing on additional COMT polymorphic sites and other candidate genes from the deleted region will elucidate the molecular pathways leading to schizophrenia and other psychiatric disorders in VCFS.]. 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:16734939
;
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:NP258925.RAemTTdcyKPC7np8yO1niTdli-bmxjJ3epdjT2xRcEMLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}