@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_assertion
a
np:Assertion
.
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a
np:Provenance
.
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a
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.
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{
miriam-gene:546
a
ncit:C16612
.
lld:C1136249
a
ncit:C7057
.
dgn-gda:DGNc35d9507c94837d2f2a294db2eb5240c
sio:SIO_000628
miriam-gene:546
,
lld:C1136249
;
a
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.
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dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_provenance
{
dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_assertion
dcterms: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_literature
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sio:SIO_000772
miriam-pubmed:19291773
;
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 .
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dgn-np:NP726570.RAVrgRmIXYuQsp9Ig8CdX9nLj34TY9cgdihYrd5bi956g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:14+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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pav:authoredBy
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> , <
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> , <
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