@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M
> .
@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:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_head
{
this:
np:hasAssertion
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_assertion
;
np:hasProvenance
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_provenance
;
np:hasPublicationInfo
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_assertion
a
np:Assertion
.
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_provenance
a
np:Provenance
.
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0026106
a
ncit:C7057
.
dgn-gda:DGN632eb3cb22ca5d5558808644ea367b84
sio:SIO_000628
miriam-gene:4204
,
lld:C0026106
;
a
sio:SIO_001121
.
}
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_provenance
{
dgn-np:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_assertion
dcterms:description
"[Molecular analysis has allowed the phenotype of MECP2 mutations to be broadened beyond RTT to include girls who have mild mental retardation, autism, and an Angelman syndrome phenotype, as well as males with severe encephalopathy.]. 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:12210319
;
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:NP366762.RAj2nn0OiYN67OM8TGbPKqjpIBiqJPD1UzYGU3D0iWF9M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:31+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" .
}