@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_head
{
this:
np:hasAssertion
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_assertion
;
np:hasProvenance
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_assertion
a
np:Assertion
.
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_provenance
a
np:Provenance
.
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNb67773e529a8580582ce6c01dacf229d
sio:SIO_000628
miriam-gene:367
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_provenance
{
dgn-np:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_assertion
dcterms:description
"[In addition, autistic female brain DNA samples showed evidence for aberrant MECP2 promoter methylation as an increase in the number of bisulfite sequenced clones with undefined XCI status for MECP2 but not androgen receptor (AR).]. 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:19132145
;
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:NP373080.RAHx0XOENDF-nGAUa9J1CGsdrEmqoqVRTe-3B3FjUtg5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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: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" .
}