@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ
> .
@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:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_head
{
this:
np:hasAssertion
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion
;
np:hasProvenance
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion
a
np:Assertion
.
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance
a
np:Provenance
.
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNb49acb79496f7fab891c80f6568a0120
sio:SIO_000628
miriam-gene:7015
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_provenance
{
dgn-np:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_assertion
dcterms:description
"[Due to the systemic involvement of telomerase diseases very likely influencing the clinical outcome, and the peculiar biological features of hepatocellular carcinoma arising in this context, we suggest that patients with cryptogenic cirrhosis or other suggestive features should be screened for TERT mutations and specific treatment algorithms elaborated for this disease.]. 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:23000435
;
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:NP174449.RAgtGCh3Q9aBZ42gfkhdD6WSJu6Jg23OUW3AHnOMVwSFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}