@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ
> .
@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:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_head
{
this:
np:hasAssertion
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_assertion
;
np:hasProvenance
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_assertion
a
np:Assertion
.
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_provenance
a
np:Provenance
.
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_assertion
{
miriam-gene:6712
a
ncit:C16612
.
lld:C0004134
a
ncit:C7057
.
dgn-gda:DGN7105dc9e739237676f033706313af451
sio:SIO_000628
miriam-gene:6712
,
lld:C0004134
;
a
sio:SIO_001121
.
}
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_provenance
{
dgn-np:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_assertion
dcterms:description
"[We also examined a mouse knockout of β-III spectrin in which ataxia and progressive degeneration of cerebellar Purkinje cells has been previously reported and found morphological abnormalities in neurons from prefrontal cortex and deficits in object recognition tasks, consistent with the human cognitive phenotype.]. 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:23236289
;
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:NP891614.RAPwLH7tM6cjcYOuWKVGPa2Wc887mJexhqDvsBSPZniJQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}