@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w
> .
@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:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_head
{
this:
np:hasAssertion
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_assertion
;
np:hasProvenance
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_assertion
a
np:Assertion
.
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_provenance
a
np:Provenance
.
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_assertion
{
miriam-gene:653820
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGNbd37debdd9cca4e42ae5159ddbcea8c1
sio:SIO_000628
miriam-gene:653820
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_provenance
{
dgn-np:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_assertion
dcterms:description
"[Overall, three of 99 gastric cancers (3%) were found to have the caspase-10 mutations, which were identified in the coding regions of the death effector domain (codon 147) and the p17 large protease domain (codons 257 and 410), whereas no mutation was detected in caspase-8.]. 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:11973654
;
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:NP265496.RAaL9C74fbcv_t8QGj_xq-DdZ_-LJTZE9fY9uZ0Xvvb2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}