@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8
> .
@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:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_head
{
this:
np:hasAssertion
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_assertion
;
np:hasProvenance
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_assertion
a
np:Assertion
.
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_provenance
a
np:Provenance
.
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_assertion
{
miriam-gene:259266
a
ncit:C16612
.
lld:C0431350
a
ncit:C7057
.
dgn-gda:DGNa95a3bf50b0ceef21ed71ca797d24dd0
sio:SIO_000628
miriam-gene:259266
,
lld:C0431350
;
a
sio:SIO_001121
.
}
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_provenance
{
dgn-np:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_assertion
dcterms:description
"[Here we show that the most common cause of MCPH is homozygous mutation of ASPM, the human ortholog of the Drosophila melanogaster abnormal spindle gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts.]. 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:12355089
;
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:NP248479.RA1pjWvLBuO-pZBa2bVKlYO6fst6jZ9eG8JvVxyKe8cK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}