@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA
> .
@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:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_head
{
this:
np:hasAssertion
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_assertion
;
np:hasProvenance
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_provenance
;
np:hasPublicationInfo
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_assertion
a
np:Assertion
.
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_provenance
a
np:Provenance
.
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_assertion
{
miriam-gene:64478
a
ncit:C16612
.
lld:C0345904
a
ncit:C7057
.
dgn-gda:DGN5b78c5719a0b4ec6984c911d51994c01
sio:SIO_000628
miriam-gene:64478
,
lld:C0345904
;
a
sio:SIO_001121
.
}
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_provenance
{
dgn-np:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_assertion
dcterms:description
"[1q gain and 1p and 17p LOH are early molecular events, whereas gains in 5q and 8q and LOH on 4q and 8p only occur in advanced HCC, and inactivation of the putative suppressor gene, CSMD1, may be the key event in progression of liver cancer.]. 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:19105209
;
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:NP805469.RAZUTr5Pa6Vw4RKIl9_uTcoxhUJMS09ctMA9Blj8Qq4CA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}