@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI
> .
@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:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_assertion
;
np:hasProvenance
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_provenance
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np:hasPublicationInfo
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_assertion
a
np:Assertion
.
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_provenance
a
np:Provenance
.
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:10984
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNafc613de83f365ec3b2203139a5a9da0
sio:SIO_000628
miriam-gene:10984
,
lld:C0006826
;
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.
}
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_provenance
{
dgn-np:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_assertion
dcterms:description
"[We have found that loss of imprinting (LOI) of the autocrine growth factor gene IGF2 and of the untranslated antisense RNA LIT1, within the K(V)LQT1 gene, account for most cases of BWS, and that cancer risk is specifically associated with LOI of IGF2.]. 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:16869770
;
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:NP211631.RALc-TE2rnsNy1PH43_R7Z87rFjkzXcIWnhmHph-3i8FI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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