@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4
> .
@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:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_head
{
this:
np:hasAssertion
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_assertion
;
np:hasProvenance
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_provenance
;
np:hasPublicationInfo
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_assertion
a
np:Assertion
.
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_provenance
a
np:Provenance
.
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN33d2de603790f7ce892c89267a9d95d9
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_provenance
{
dgn-np:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_assertion
dcterms:description
"[In this study we summarize the results of diagnostic testing of 30 patients with Rett syndrome (RTT) or mental retardation of unknown etiology using bidirectional sequencing of the open reading frame of the MECP2 gene.]. 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:22277191
;
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:NP956004.RAcSEeAauDCrRaD05y8kcuwchsG9W2sxE9cJ0PeACBno4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:58+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" .
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pav:version
"v4.0.0" .
}