@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg
> .
@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:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_head
{
this:
np:hasAssertion
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_assertion
;
np:hasProvenance
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_assertion
a
np:Assertion
.
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_provenance
a
np:Provenance
.
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_assertion
{
miriam-gene:3423
a
ncit:C16612
.
lld:C0026705
a
ncit:C7057
.
dgn-gda:DGN106114f7605088ffa46ad8e707212460
sio:SIO_000628
miriam-gene:3423
,
lld:C0026705
;
a
sio:SIO_001124
.
}
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_provenance
{
dgn-np:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_assertion
dcterms:description
"[These findings suggest methylation patterns in the beginning of IDS genomic region are polymorphic in humans and that hypermethylation in this region in some individuals predisposes them to CpG mutations resulting in Hunter syndrome.]. 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:16617305
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP216668.RAZhRQpZUV8tNQI9YI5cPtafelq8hudONEF51IgEDBgTg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:25+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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}