@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8
> .
@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 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:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_head
{
this:
np:hasAssertion
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_assertion
;
np:hasProvenance
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_provenance
;
np:hasPublicationInfo
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_assertion
a
np:Assertion
.
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_provenance
a
np:Provenance
.
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_assertion
{
miriam-gene:546
a
ncit:C16612
.
lld:C1136249
a
ncit:C7057
.
dgn-gda:DGNda13e031f3fd3012664ec262754c73ed
sio:SIO_000628
miriam-gene:546
,
lld:C1136249
;
a
sio:SIO_001121
.
}
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_provenance
{
dgn-np:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_assertion
dc:description
"[Detailed comparison of the clinical characteristics and the function of the genes located in the commonly duplicated regions of these patients led us to the hypothesis that an increased dosage of ATRX and perhaps of other genes is involved in the pathogenetic mechanism of this XLMR phenotype, including mental retardation, short stature, and genital abnormalities comprising cryptorchidism and/or a small penis.]. 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:19291773
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
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:NP9480.RAeAchc58HyI6p-_Jp2ZI77tQ1PXzjPUFY6OZwsfxFpW8130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:02+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}