@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0
> .
@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:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_head
{
this:
np:hasAssertion
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_assertion
;
np:hasProvenance
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_assertion
a
np:Assertion
.
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_provenance
a
np:Provenance
.
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_assertion
{
miriam-gene:3984
a
ncit:C16612
.
lld:C0679466
a
ncit:C7057
.
dgn-gda:DGN7597ae9da760b872d781b19d1a35132c
sio:SIO_000628
miriam-gene:3984
,
lld:C0679466
;
a
sio:SIO_001121
.
}
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_provenance
{
dgn-np:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_assertion
dcterms:description
"[These findings rule out the claim that the deletion of one copy of LIMK1 is alone sufficient to result in spatial impairment, but leave open the possibility that LIMK1 contributes to the WS cognitive deficits if deleted in combination with other genes within the WS deletion.]. 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:16216290
;
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:NP658990.RAxQkaQ4Z50cASFYbI7qH5p8wXG-2t0Bp0Wn1P8HX5q_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}