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> .
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> .
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http://www.w3.org/2001/XMLSchema#
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://linkedlifedata.com/resource/umls/id/
> .
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
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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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{
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np:Assertion
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miriam-gene:6586
a
ncit:C16612
.
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a
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.
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dgn-np:NP702101.RAkWCDyuEcCe5dpoo7fIKg4EyFI42op9UdOSi_kDjhHrY130_assertion
dcterms:description
"[Based on this, we also propose three novel dyslexia candidate genes (SLIT2, HMGB1 and VAPA) from known linkage regions, and we discuss the possible involvement of genes emerging from the two reported genome-wide association studies for reading impairment-related phenotypes in the identified network.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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.
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xsd:date
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dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
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{
this:
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xsd:dateTime
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> , <
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