@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_head
{
this:
np:hasAssertion
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_assertion
;
np:hasProvenance
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_assertion
a
np:Assertion
.
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_provenance
a
np:Provenance
.
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_assertion
{
miriam-gene:7051
a
ncit:C16612
.
lld:C0175693
a
ncit:C7057
.
dgn-gda:DGNf6922b601d41c737b8df29f6bcd45c0a
sio:SIO_000628
miriam-gene:7051
,
lld:C0175693
;
a
sio:SIO_001121
.
}
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_provenance
{
dgn-np:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_assertion
dcterms:description
"[To show whether general hypomethylation is a common phenomenon in imprinting disorders we carried out methylation analyses for the imprinted regions 14q32, 6q24 and the centromeric imprinting region ICR2 on 11p15 for 10 patients with SRS carrying mUPD7 and 22 patients with LOM at the telomeric imprinting region ICR1.]. 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:18341093
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP801317.RAf0sRLe1tJlRrpIeHnfi_4gRzvKit-R_Rr9uXMxNM5CQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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: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" .
}