@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU
> .
@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/v3.0.0/void/
> .
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_head
{
this:
np:hasAssertion
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_assertion
;
np:hasProvenance
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_assertion
a
np:Assertion
.
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_provenance
a
np:Provenance
.
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN3fd1377554331bcf973f5b2fecf5a18e
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_provenance
{
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_assertion
dcterms:description
"[Taking advantage of the nonrandom pattern of X chromosome inactivation in female induced pluripotent stem cells (iPSC), we have generated isogenic pairs of wild type and mutant iPSC lines from several female RTT patients with common and rare RTT mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:21966470
;
prov:wasDerivedFrom
dgn-void:ctd_human-20150221
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20150221
pav:importedOn
"2015-02-21"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP21807.RAgWONYJ8bLjvfxs1Jn1aQ8ytzqg6ffLbYAleusfFwdkU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:37:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}