@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_assertion
;
np:hasProvenance
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_provenance
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np:hasPublicationInfo
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_assertion
a
np:Assertion
.
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_provenance
a
np:Provenance
.
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_assertion
{
miriam-gene:1781
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGN067f29521eeaae13d9623220df6f73df
sio:SIO_000628
miriam-gene:1781
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_provenance
{
dgn-np:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_assertion
dcterms:description
"[As loss of methylation at imprinting control regions other than 11p15.5 might modify the phenotype of BWS patients with IC2 epimutations, we investigated differentially methylated regions (DMRs) at 6q24, 7q32 and 15q13 in post-ART and non-ART BWS IC2 cases (n = 55).]. 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:19073614
;
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:NP499327.RAsFd26WZRu4wtsX2Nti9OVzY4i71mJ21tqB5tg7gLL8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}