@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ
> .
@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:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_head
{
this:
np:hasAssertion
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_assertion
;
np:hasProvenance
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_assertion
a
np:Assertion
.
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_provenance
a
np:Provenance
.
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_assertion
{
miriam-gene:581
a
ncit:C16612
.
lld:C1704273
a
ncit:C7057
.
dgn-gda:DGN5b333ca7970c0ce97a55baae635bb600
sio:SIO_000628
miriam-gene:581
,
lld:C1704273
;
a
sio:SIO_001121
.
}
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_provenance
{
dgn-np:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_assertion
dcterms:description
"[To understand the roles of these genes in hereditary nonpolyposis colorectal cancer (HNPCC) tumorigenesis, we examined whether BAX mutations occur in adenoma and carcinoma specimens from patients with HNPCC and also determined the frequencies of p53 mutations.]. 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:9453486
;
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:NP845312.RAK_9OC4rQA-CFNSi_ybcJa0xlrX3w8cXhtMgcrtHVhGQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}