@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA
> .
@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/
> .
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_head
{
this:
np:hasAssertion
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_assertion
;
np:hasProvenance
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_provenance
;
np:hasPublicationInfo
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_assertion
a
np:Assertion
.
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_provenance
a
np:Provenance
.
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_assertion
{
miriam-gene:203068
a
ncit:C16612
.
lld:C1955869
a
ncit:C7057
.
dgn-gda:DGNd9a3087b7bc7fa79ad55ac25d5f3aa04
sio:SIO_000628
miriam-gene:203068
,
lld:C1955869
;
a
sio:SIO_001121
.
}
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_provenance
{
dgn-np:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_assertion
dcterms:description
"[Inputs from genetic studies were provided through the identification of several mutated genes encoding either proteins associated with microtubules (DCX, LIS1, KIF2A, KIF5C, DYNC1H1) or tubulin subunits (TUBA1A, TUBB2B, TUBB5 and TUBG1), in malformations of cortical development (MCD).]. 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:24179174
;
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:NP979716.RA6vYJiIhJww7xF5kFCC9QV48GriWb7Ap3IrMvGxCcAIA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:38+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}