@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM
> .
@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:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_head
{
this:
np:hasAssertion
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_assertion
;
np:hasProvenance
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_assertion
a
np:Assertion
.
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_provenance
a
np:Provenance
.
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNac1e9c2266874a93606c3d0cde8f7619
sio:SIO_000628
miriam-gene:7157
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_provenance
{
dgn-np:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_assertion
dcterms:description
"[A number of recently published NGS studies on HCCs have not only confirmed previously known mutations in CTNNB1 and TP53 in HCC, but also identified novel genetic alterations in HCC including mutations in genes involved in epigenetic regulation.]. 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:23063663
;
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:NP1020676.RAyaAcjup_RIi_vvE0IGxRe3lctSjsaVoih0TMtEd3tVM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:28+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: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" .
}