@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I
> .
@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:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_head
{
this:
np:hasAssertion
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_assertion
;
np:hasProvenance
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_provenance
;
np:hasPublicationInfo
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_assertion
a
np:Assertion
.
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_provenance
a
np:Provenance
.
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_assertion
{
miriam-gene:7461
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN0735061d3bf2a6997be9920c60be4c6b
sio:SIO_000628
miriam-gene:7461
,
lld:C0175702
;
a
sio:SIO_001121
.
}
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_provenance
{
dgn-np:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_assertion
dcterms:description
"[The hemideletion of approximately 25 genes on chromosome 7q11.23 that causes Williams syndrome (WS) includes genes that regulate cytoskeletal dynamics in neurons, especially LIMK1 and CYLN2, and therefore offers the opportunity to investigate the role of these genes in the formation of white matter tracts.]. 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:17827280
;
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:NP796726.RA3qBm-48_U5lk6FU9haT7RAbm9WIFkbkX5ignL2IFP2I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}