@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk
> .
@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/v4.0.0/void/
> .
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_head
{
this:
np:hasAssertion
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_assertion
;
np:hasProvenance
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_provenance
;
np:hasPublicationInfo
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_assertion
a
np:Assertion
.
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_provenance
a
np:Provenance
.
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_assertion
{
miriam-gene:51473
a
ncit:C16612
.
lld:C0476254
a
ncit:C7057
.
dgn-gda:DGN64d38417cf45da5bf05dd79302f6af9b
sio:SIO_000628
miriam-gene:51473
,
lld:C0476254
;
a
sio:SIO_001121
.
}
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_provenance
{
dgn-np:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_assertion
dcterms:description
"[We observed a slight tendency for an intronic deletion in DCDC2 to be associated with worse performance on some quantitative measures of dyslexia in the probands in our sample, but not in their parents.]. 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:17450541
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP605824.RA87LELiWgtwaGvWb0JINhaZCM-9wX1FAQpcvpVgo9mOk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:20+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}