@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww
> .
@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:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_head
{
this:
np:hasAssertion
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_assertion
;
np:hasProvenance
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_provenance
;
np:hasPublicationInfo
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_assertion
a
np:Assertion
.
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_provenance
a
np:Provenance
.
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_assertion
{
miriam-gene:4684
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGN93109aba85e777050111d0862c21b4ff
sio:SIO_000628
miriam-gene:4684
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_provenance
{
dgn-np:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_assertion
dcterms:description
"[We found that SNPs within the LPHN3 gene interact with SNPs spanning the 11q region that contains DRD2 and NCAM1 not only to increase the risk of developing ADHD but also to increase ADHD severity.]. 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:22832519
;
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:NP688070.RADAw-g3O6mEFRfmt0TV0QN94g6i9QGNP0uglCr5-g7ww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}