@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8
> .
@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:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_head
{
this:
np:hasAssertion
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_assertion
;
np:hasProvenance
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_assertion
a
np:Assertion
.
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_provenance
a
np:Provenance
.
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_assertion
{
miriam-gene:10165
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN975224e3d560d4d80234080cb4c61f8d
sio:SIO_000628
miriam-gene:10165
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_provenance
{
dgn-np:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_assertion
dcterms:description
"[Because CTLN2 has been associated with hepatocellular carcinoma (HCC) and may be involved in hepatocarcinogenesis, the objective of this study was to assess the frequency of SLC25A13 mutations in patients with non-viral HCC.]. 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:21470889
;
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:NP623735.RA-vdDkdIpCefQAtbtpcM-3QhyUk7MYMb-qIIqzJ5ywi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}