@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo
> .
@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:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_assertion
a
np:Assertion
.
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_provenance
a
np:Provenance
.
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3146
a
ncit:C16612
.
lld:C0476254
a
ncit:C7057
.
dgn-gda:DGNe0ab6a09a4b9da6e9ea90b44a432f440
sio:SIO_000628
miriam-gene:3146
,
lld:C0476254
;
a
sio:SIO_001121
.
}
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_provenance
{
dgn-np:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_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 ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:20956978
;
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:NP459520.RAt9U8tOL0mFW4mEZe83_5ftIj0ItevJH16Q6i801kmyo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:09+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
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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" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
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