@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion
a
np:Assertion
.
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance
a
np:Provenance
.
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion
{
miriam-gene:161582
a
ncit:C16612
.
lld:C0476254
a
ncit:C7057
.
dgn-gda:DGNf2d995f661a23668d4eb88c93662cd09
sio:SIO_000628
miriam-gene:161582
,
lld:C0476254
;
a
sio:SIO_001121
.
}
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance
{
dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion
dcterms:description
"[Within two of these loci, DYX1C1 (15q21) and ROBO1 (3p12) have recently been proposed as dyslexia candidate genes through the molecular analysis of translocation breakpoints in dyslexic individuals carrying balanced chromosomal translocations.]. 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:18521840
;
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:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:37+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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" .
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pav:version
"v3.0.0" .
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