@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M
> .
@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:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_head
{
this:
np:hasAssertion
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_assertion
;
np:hasProvenance
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_provenance
;
np:hasPublicationInfo
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_assertion
a
np:Assertion
.
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_provenance
a
np:Provenance
.
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_assertion
{
miriam-gene:2477
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN9ef538f432b6331e45b88c3bd6cb6461
sio:SIO_000628
miriam-gene:2477
,
lld:C0175702
;
a
sio:SIO_001121
.
}
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_provenance
{
dgn-np:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_assertion
dcterms:description
"[The purpose of this prospective study was to compare and contrast age related to cognitive abilities, adaptive and maladaptive behaviors in children and adolescents in the same age range, diagnosed with one of three genetic disorders: the FRAXA mutation, Neurofibromatosis type 1 (NF1) or Williams-Beuren syndrome (WBS).]. 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:17853466
;
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:NP833621.RAPPSf20T_htaesFmdEEGOiGQDNzMvHq0w07taUcn_Q8M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}