@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw
> .
@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:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_head
{
this:
np:hasAssertion
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_assertion
;
np:hasProvenance
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_provenance
;
np:hasPublicationInfo
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_assertion
a
np:Assertion
.
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_provenance
a
np:Provenance
.
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0032131
a
ncit:C7057
.
dgn-gda:DGNe3223924b00f7bc47980638ed3acb1ad
sio:SIO_000628
miriam-gene:6520
,
lld:C0032131
;
a
sio:SIO_001121
.
}
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_provenance
{
dgn-np:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_assertion
dcterms:description
"[Since the IgH switch recombination and somatic hypermutation mechanism are turned off in plasma cells and plasma cell tumors, the MYC rearrangements are thought to be mediated by unknown mechanisms that contribute to structural genomic instability in all kinds of tumors.]. 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:16829212
;
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:NP738345.RAEsOOHgf1yKu4-wz2lmKVN2WlbCdZYfdxXaBlbqdC6Jw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}