@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0
> .
@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/v4.0.0/void/
> .
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_head
{
this:
np:hasAssertion
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_assertion
;
np:hasProvenance
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_assertion
a
np:Assertion
.
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_provenance
a
np:Provenance
.
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_assertion
{
miriam-gene:259266
a
ncit:C16612
.
lld:C3711387
a
ncit:C7057
.
dgn-gda:DGNfdfe80282bcf4c3731d3bae949af8523
sio:SIO_000628
miriam-gene:259266
,
lld:C3711387
;
a
sio:SIO_001121
.
}
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_provenance
{
dgn-np:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP369301.RAeW7mF-LNVwIX_MefDFI5fEZ1IqAXniW7BHttg1fZrH0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:32+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}