@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno
> .
@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 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:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_head
{
this:
np:hasAssertion
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_assertion
;
np:hasProvenance
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_provenance
;
np:hasPublicationInfo
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_assertion
a
np:Assertion
.
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_provenance
a
np:Provenance
.
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_assertion
{
miriam-gene:1749
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNe174d28a1381bd1e11460bf53099f988
sio:SIO_000628
miriam-gene:1749
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_provenance
{
dgn-np:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_assertion
dct:description
"[Decreased dendritic arborization is common to RS and autism, leading to further research on similarities in pathogenesis, including MeCP2 protein levels in autistic brains and MeCP2 effects on genes connected to autism, like DLX5 and genes on 15q11-13 region.]. 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:17562589
;
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:NP936537.RAJl9Sb2jd7W2SBp32p06s7qxtwV_cOjBKuMUrKQroFno130_publicationInfo
{
this:
dct:created
"2014-10-02T12:41:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}