@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4
> .
@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:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_head
{
this:
np:hasAssertion
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_assertion
;
np:hasProvenance
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_provenance
;
np:hasPublicationInfo
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_assertion
a
np:Assertion
.
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_provenance
a
np:Provenance
.
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_assertion
{
miriam-gene:23135
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNb7ab51dc0847c81aaad5d0c50dfc0bf0
sio:SIO_000628
miriam-gene:23135
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_provenance
{
dgn-np:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_assertion
dcterms:description
"[This analysis also revealed that most HNSCC cells harbor multiple mutations and CNVs in epigenetic modifiers (e.g., EP300, CREBP, MLL1, MLL2, MLL3, KDM6A, and KDM6B) that may contribute to HNSCC initiation and progression.]. 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:25275298
;
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:NP1225660.RAqDbCCnAIZvaC8iGROBUQUOz2K0vTTlH_i9emWqtrlU4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:01+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" .
}