@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA
> .
@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:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_head
{
this:
np:hasAssertion
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_assertion
;
np:hasProvenance
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_assertion
a
np:Assertion
.
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_provenance
a
np:Provenance
.
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN3c87bd894af5ce70989c4ea56733f1da
sio:SIO_000628
miriam-gene:3342
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_provenance
{
dgn-np:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_assertion
dcterms:description
"[By comparative genomic hybridisation (CGH) 40 cases, including cirrhotic liver (CL), focal nodular hyperplasia (FNHs), hepatocellular adenoma (HCAs), dysplastic nodules (DNs), primary hepatocellular carcinoma (HCCs), and hepatocellular metastases to the lung were studied.]. 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:15030983
;
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:NP417358.RAo3s5QG-r0WSuRV69SkHpmfZiKWeGD6vaHadyiJ0DQUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}