@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY
> .
@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:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_head
{
this:
np:hasAssertion
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion
;
np:hasProvenance
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion
a
np:Assertion
.
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance
a
np:Provenance
.
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion
{
miriam-gene:7846
a
ncit:C16612
.
lld:C0266470
a
ncit:C7057
.
dgn-gda:DGNb910544a3ffbdd1b725b509682ce79a6
sio:SIO_000628
miriam-gene:7846
,
lld:C0266470
;
a
sio:SIO_001121
.
}
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance
{
dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion
dcterms:description
"[All together, it emerges that the TUBA1A related lissencephaly spectrum ranges from perisylvian pachygyria, in the less severe form, to posteriorly predominant pachygyria in the most severe, associated with dysgenesis of the anterior limb of the internal capsule and mild to severe cerebellar hypoplasia.]. 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:18728072
;
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:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}