@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw
> .
@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:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_head
{
this:
np:hasAssertion
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_assertion
;
np:hasProvenance
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_provenance
;
np:hasPublicationInfo
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_assertion
a
np:Assertion
.
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_provenance
a
np:Provenance
.
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_assertion
{
miriam-gene:55755
a
ncit:C16612
.
lld:C0025958
a
ncit:C7057
.
dgn-gda:DGNec04cd161a041dd05f864d7571f1891e
sio:SIO_000628
miriam-gene:55755
,
lld:C0025958
;
a
sio:SIO_001121
.
}
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_provenance
{
dgn-np:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_assertion
dcterms:description
"[We integrate the impact of centriole replication defects with the functions of Cdk5rap2 and other MCPH proteins, propose mechanisms for progenitor loss in MCPH, and discuss links to two other microcephaly syndromes.]. 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:21632253
;
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:NP752582.RACumHsLEaQUceCD2RbmdB8A48KAPg5KJMTC4L1jf_0Bw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}