@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo
> .
@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:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_head
{
this:
np:hasAssertion
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_assertion
;
np:hasProvenance
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_provenance
;
np:hasPublicationInfo
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_assertion
a
np:Assertion
.
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_provenance
a
np:Provenance
.
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_assertion
{
miriam-gene:7178
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8b74ca009f46e889c39a03bee9b9ef53
sio:SIO_000628
miriam-gene:7178
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_provenance
{
dgn-np:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_assertion
dcterms:description
"[Studying these extremely rare events of tumour reversion and deciphering these pathways, which involve SIAH1, presenilin 1, TSAP6 and translationally controlled tumour protein (TCTP), could lead to new avenues in cancer treatment.]. 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:19180095
;
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:NP817732.RAQfaQhe3RfPEpS0KfvYSjfoxI6vgMtrtG0QuO57Ukplo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}