@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ
> .
@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:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_head
{
this:
np:hasAssertion
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_assertion
;
np:hasProvenance
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_assertion
a
np:Assertion
.
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_provenance
a
np:Provenance
.
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_assertion
{
miriam-gene:2018
a
ncit:C16612
.
lld:C0266484
a
ncit:C7057
.
dgn-gda:DGNea4cc90f275700197acdb51b8ebef0f0
sio:SIO_000628
miriam-gene:2018
,
lld:C0266484
;
a
sio:SIO_001121
.
}
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_provenance
{
dgn-np:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_assertion
dcterms:description
"[The present findings, together with the reported cases of schizencephaly associated with EMX2 mutations, support the hypothesis that, at least in some cases, schizencephalies are determined by deleterious mutations of this homeobox gene.]. 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:9153481
;
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:NP582878.RApQhPSvkQ3yL2rD5hnvt00YlSzbXU7jTuTo89ogzUXgQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}