@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ
> .
@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:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_head
{
this:
np:hasAssertion
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_assertion
;
np:hasProvenance
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_assertion
a
np:Assertion
.
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_provenance
a
np:Provenance
.
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_assertion
{
miriam-gene:56259
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN989366404e764d92516feffe2c789723
sio:SIO_000628
miriam-gene:56259
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_provenance
{
dgn-np:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_assertion
dcterms:description
"[These results suggest that p14(ARF), p16(INK4a) and p53 are differentially disrupted through distinct molecular mechanisms at different stages in HCC and that p14(ARF) and p53 appear to function in the same tumor suppression pathway in HCC]. 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:12168936
;
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:NP213171.RA7pzHvocNViHkG_vwT1rj_kJOT7JBzG-LDcJXnhdKUHQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}