@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k
> .
@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:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_head
{
this:
np:hasAssertion
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion
;
np:hasProvenance
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion
a
np:Assertion
.
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance
a
np:Provenance
.
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion
{
miriam-gene:23705
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN68ef15dfa9d8a08a8f492490eeaa3730
sio:SIO_000628
miriam-gene:23705
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_provenance
{
dgn-np:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_assertion
dcterms:description
"[Bisulphite sequencing and genetic analysis of 18 primary neuroblastomas suggested that neither haploinsufficiency nor hypermethylation is regularly involved in CADM1 gene silencing in neuroblastoma, which is in contrast to results obtained in other malignancies.]. 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:18084322
;
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:NP606878.RADEC8_I1bXNHXvOt2digGiZ5oxvGuLvMK1cAeufz5h_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}