@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ
> .
@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:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_head
{
this:
np:hasAssertion
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_assertion
;
np:hasProvenance
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_assertion
a
np:Assertion
.
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_provenance
a
np:Provenance
.
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_assertion
{
miriam-gene:170302
a
ncit:C16612
.
lld:C0085584
a
ncit:C7057
.
dgn-gda:DGN3741b5c60efb314c998eeda754518846
sio:SIO_000628
miriam-gene:170302
,
lld:C0085584
;
a
sio:SIO_001121
.
}
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_provenance
{
dgn-np:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_assertion
dcterms:description
"[Recently, it has been reported that longer expansions of the polyalanine tract of the ARX gene could cause an early infantile encephalopathy with suppression burst pattern and that the length of this repeat region could be related to the severity of the electroclinical picture.]. 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:21108397
;
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:NP336647.RA4IqvVCkjUiRUIS484ZS0SlEGRsmcydRg2RLpq2UNyWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}