@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg
> .
@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:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_head
{
this:
np:hasAssertion
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_assertion
;
np:hasProvenance
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_assertion
a
np:Assertion
.
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_provenance
a
np:Provenance
.
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_assertion
{
miriam-gene:7531
a
ncit:C16612
.
lld:C0266463
a
ncit:C7057
.
dgn-gda:DGNf4bd56440908d8322bc31a754623dbc3
sio:SIO_000628
miriam-gene:7531
,
lld:C0266463
;
a
sio:SIO_001121
.
}
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_provenance
{
dgn-np:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_assertion
dcterms:description
"[On the basis of recent functional data and the creation of a mouse model suggesting a role for 14-3-3 epsilon in cortical development, we suggest that deletion of one or both of these genes in combination with deletion of LIS1 may contribute to the more severe form of lissencephaly seen only in patients with MDS.]. 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:12621583
;
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:NP726065.RAxpGmOcmam06USweGxTKuArpmWqTY4DGWr149__Q5kSg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}