@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs
> .
@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/v4.0.0/void/
> .
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_head
{
this:
np:hasAssertion
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_assertion
;
np:hasProvenance
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_provenance
;
np:hasPublicationInfo
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_assertion
a
np:Assertion
.
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_provenance
a
np:Provenance
.
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_assertion
{
miriam-gene:2026
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN4908051ae99d28b980e0ae9a6e55b81a
sio:SIO_000628
miriam-gene:2026
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_provenance
{
dgn-np:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_assertion
dcterms:description
"[These results suggest that most RTT phenotypes are caused either by disruption of complex neural networks involving neurons throughout the brain or by disruption of the function of specific neurons outside of the broad CamKII or Eno2 distribution.]. 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:17635839
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP620413.RAF0dJDRV9CUHrLukZsweg2KOnma_m3uHQRnhdozZONGs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:27+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}