@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA
> .
@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:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_head
{
this:
np:hasAssertion
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_assertion
;
np:hasProvenance
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_provenance
;
np:hasPublicationInfo
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_assertion
a
np:Assertion
.
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_provenance
a
np:Provenance
.
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_assertion
{
miriam-gene:11199
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN561d0b67c6a0e1f5b7c4bb59fee194c1
sio:SIO_000628
miriam-gene:11199
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_provenance
{
dgn-np:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_assertion
dcterms:description
"[In conclusion, the aberrant expressions of AFP, OPN and ANXA10S cooperatively contribute to tumor progression and poor prognosis, and are useful for molecular staging of HCC and the subclassification of stage II HCC without vascular invasion.]. 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:15754002
;
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:NP666352.RAc6ROhoBHsjn2MR5zY2mDsKgBlARdRO2mJc1X9BoDZXA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}