@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_head
{
this:
np:hasAssertion
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_assertion
;
np:hasProvenance
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_provenance
;
np:hasPublicationInfo
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_assertion
a
np:Assertion
.
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_provenance
a
np:Provenance
.
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C3825704
a
ncit:C7057
.
dgn-gda:DGN862ade4c78a27414504aa69cd497797b
sio:SIO_000628
miriam-gene:1312
,
lld:C3825704
;
a
sio:SIO_001122
.
}
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_provenance
{
dgn-np:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_assertion
dcterms:description
"[We genotyped five polymorphisms at D22S941, D22S944, D22S264, and D22S311, and the COMT gene in the common 3Mbp deletion region associated with 22q11 deletion syndrome in 300 Japanese schizophrenics and 300 controls and identified one patient with 22q11 deletion (Arinami et al., 2001).]. 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:11705709
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP322317.RA1G0Z8p1zQ_u-QdrLIIiLPNQRD5ZrqcWB2-IPahde3Qw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:45+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}