@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM
> .
@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:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_head
{
this:
np:hasAssertion
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_assertion
;
np:hasProvenance
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_provenance
;
np:hasPublicationInfo
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_assertion
a
np:Assertion
.
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_provenance
a
np:Provenance
.
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_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:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_provenance
{
dgn-np:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_assertion
dcterms:description
"[ADHD occurred more frequently in association with mutations predicted to affect Dp140 expression (exon 45-55) and in those with mutations predicted to affect all dystrophin product, including Dp71 (ie, those that have promoter region and specific first exon between exons 62 and 63 but were also relatively frequent).]. 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-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:NP311333.RAzr4ROR1hTHfNl11ScqbSM9530DshZU3Rqp1HO-gOCGM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}