@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc
> .
@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:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_head
{
this:
np:hasAssertion
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_assertion
;
np:hasProvenance
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_provenance
;
np:hasPublicationInfo
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_assertion
a
np:Assertion
.
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_provenance
a
np:Provenance
.
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGN6e0894527ee2b4dcda1d7c3170341ff1
sio:SIO_000628
miriam-gene:1756
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_provenance
{
dgn-np:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_assertion
dcterms:description
"[The risk of ADHD appears to be higher in patients carrying mutations predicted to affect dystrophin isoforms expressed in the brain and are known to be associated with higher risk of cognitive impairment.]. 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:22560791
;
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:NP355628.RAXlgcxA0HvysV-2fCRL7B6OAZtWwOEWHiiYwnwtKkHpc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:05+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" .
}