@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM
> .
@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:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_head
{
this:
np:hasAssertion
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion
;
np:hasProvenance
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance
;
np:hasPublicationInfo
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion
a
np:Assertion
.
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance
a
np:Provenance
.
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion
{
miriam-gene:7461
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN950c1b63ee293940cf877211ab10214f
sio:SIO_000628
miriam-gene:7461
,
lld:C0175702
;
a
sio:SIO_001121
.
}
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance
{
dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion
dcterms:description
"[These data demonstrate abnormalities in HF in WS in agreement with murine models, implicate LIMK1 and CYLN2 in human hippocampal function, and suggest that hippocampal dysfunction may contribute to neurocognitive abnormalities in WS.]. 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:15951840
;
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:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}