@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk
> .
@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:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_head
{
this:
np:hasAssertion
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_assertion
;
np:hasProvenance
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_assertion
a
np:Assertion
.
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_provenance
a
np:Provenance
.
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0856975
a
ncit:C7057
.
dgn-gda:DGN98d47dbf92f6fa38c4019cb198018fad
sio:SIO_000628
miriam-gene:4204
,
lld:C0856975
;
a
sio:SIO_001121
.
}
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_provenance
{
dgn-np:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_assertion
dcterms:description
"[Although abnormal regulation of neuronal genes due to mutant MeCP2 is thought to induce autistic behavior and impaired development in RTT patients, precise cellular mechanisms underlying the aberrant neural progression remain unclear.]. 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:26012557
;
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:NP1285484.RA-JkT8zDyY_tFg_n-AMPvidW-71Y6MrU4KoTrN_Jn-nk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:28+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" .
}