@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU
> .
@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:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_head
{
this:
np:hasAssertion
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_assertion
;
np:hasProvenance
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_assertion
a
np:Assertion
.
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_provenance
a
np:Provenance
.
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN28dfffab1ed89024ef292ce61efe61dc
sio:SIO_000628
miriam-gene:1312
,
lld:C0004936
;
a
sio:SIO_001121
.
}
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_provenance
{
dgn-np:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_assertion
dcterms:description
"[This study demonstrated the association of a particular COMT haplotype with susceptibility to both ADHD and OCD in 22q11.2DS and supports the hypothesis that COMT gene variations contribute to genetic predisposition to psychiatric disorders in the general population.]. 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:17949513
;
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:NP239327.RAjx-aqG3VUmM1OORdo-Pzde5NM6vJzda-bYJmNSXajpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}