@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM
> .
@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:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_head
{
this:
np:hasAssertion
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_assertion
;
np:hasProvenance
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_assertion
a
np:Assertion
.
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_provenance
a
np:Provenance
.
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_assertion
{
miriam-gene:545
a
ncit:C16612
.
lld:C0025958
a
ncit:C7057
.
dgn-gda:DGN08130b52beefbe2bf0d8073d6ff61760
sio:SIO_000628
miriam-gene:545
,
lld:C0025958
;
a
sio:SIO_001121
.
}
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_provenance
{
dgn-np:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_assertion
dcterms:description
"[Important insights into human neurogenesis are being revealed by the study of rare genetic diseases that involve primary microcephaly, illustrated by the identification of the Microcephalin, abnormal spindle in microcephaly and ataxia-telangiectasia and Rad3-related genes.]. 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:15018946
;
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:NP936463.RAfAEc8dHy4uUu3tpNvVVkW3ZSMJwwtWulVnOUsjxHlFM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}