@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_head
{
this:
np:hasAssertion
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_assertion
;
np:hasProvenance
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_assertion
a
np:Assertion
.
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_provenance
a
np:Provenance
.
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_assertion
{
miriam-gene:26960
a
ncit:C16612
.
lld:C0018817
a
ncit:C7057
.
dgn-gda:DGN499900b44dca954519e0ac17589e2b59
sio:SIO_000628
miriam-gene:26960
,
lld:C0018817
;
a
sio:SIO_001121
.
}
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_provenance
{
dgn-np:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_assertion
dcterms:description
"[These findings indicate that Nbea haploinsufficiency leads to various molecular and cellular changes that affect neuroplasticity and behavioral functions in mice, and could thus underlie the ASD symptomatology in NBEA deficient humans.]. 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:23153818
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP884471.RAIF8BHhtTl_pkSzV7CkbXadMssUl_e5xkzGQxlocfa7Y130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:38+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}