@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0
> .
@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:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_head
{
this:
np:hasAssertion
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_assertion
;
np:hasProvenance
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_provenance
;
np:hasPublicationInfo
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_assertion
a
np:Assertion
.
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_provenance
a
np:Provenance
.
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0345904
a
ncit:C7057
.
dgn-gda:DGN4b3f9c6664ed68cc4420dedd8ce0c07a
sio:SIO_000628
miriam-gene:7157
,
lld:C0345904
;
a
sio:SIO_001121
.
}
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_provenance
{
dgn-np:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_assertion
dcterms:description
"[The present results suggest that accumulation of genetic changes in multiple tumor suppressor genes, especially LOH on 17p, 4q and 8p, and mutation in p53 gene, are involved in the progression of liver cancer, and LOH on 17p and 4q precedes other genetic changes.]. 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:8407553
;
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:NP496132.RAhwBsmT0qTl4hp3xNL3CcFHn-_Vv6WaHpncysJO3i-b0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}