@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM
> .
@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:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_head
{
this:
np:hasAssertion
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_assertion
;
np:hasProvenance
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_provenance
;
np:hasPublicationInfo
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_assertion
a
np:Assertion
.
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_provenance
a
np:Provenance
.
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_assertion
{
miriam-gene:8743
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN7a7a199f4caa05c4789b4a37559dfe92
sio:SIO_000628
miriam-gene:8743
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_provenance
{
dgn-np:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_assertion
dcterms:description
"[For example, a frameshift insertion/deletion (indel) is found in the coding region of TNFSF10, which disrupts the intact open reading frame and undermines the ability of TNFSF10 to induce apoptosis, in consequence promoting abnormal tumor progression.]. 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:23434521
;
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:NP644282.RAG_v0ZM-ljraXJIoWbAuuqCk7uUC3P6eGxVYqvCeX6kM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}