@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_head
{
this:
np:hasAssertion
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_assertion
;
np:hasProvenance
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_assertion
a
np:Assertion
.
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_provenance
a
np:Provenance
.
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_assertion
{
miriam-gene:6462
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNb0da6f197982fcf92ba9d475c21eb812
sio:SIO_000628
miriam-gene:6462
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_provenance
{
dgn-np:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_assertion
dcterms:description
"[Interestingly, 8q24.1 (MYC) gain, 9p21.3 (CDKN2A/2B) loss and 17p13 (TP53, ATP1B2, SAT2, SHBG) loss were recurrent genomic lesions among various types of lymphoma with clonal heterogeneity, suggesting at least in part that alterations of these genes may play a role in clonal heterogeneity.]. 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:24815991
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1181288.RAGlhT9kGPA6NCG7v3Uiw0MTledoSOpH_aZ8N8Pgj7aJo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:41+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}