@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg
> .
@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:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_head
{
this:
np:hasAssertion
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_assertion
;
np:hasProvenance
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_assertion
a
np:Assertion
.
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_provenance
a
np:Provenance
.
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0279000
a
ncit:C7057
.
dgn-gda:DGNeb5f636b2deae63da17016e18dd50f1d
sio:SIO_000628
miriam-gene:7248
,
lld:C0279000
;
a
sio:SIO_001121
.
}
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_provenance
{
dgn-np:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_assertion
dcterms:description
"[Loss of heterozygosity (LOH) on chromosome 13q is one of the most common genetic alterations in hepatocellular carcinoma (HCC) and might be involved in liver cancer development through inactivation of tumour suppressor genes.]. 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:10674021
;
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:NP199380.RAOseLXKm5sbM2841IAb0z_dqU0SxdoOjdT3eY6VBOHwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}