@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug
> .
@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:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_head
{
this:
np:hasAssertion
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_assertion
;
np:hasProvenance
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_provenance
;
np:hasPublicationInfo
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_assertion
a
np:Assertion
.
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_provenance
a
np:Provenance
.
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_assertion
{
miriam-gene:6794
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN37ab236799bd775b082dfa77081ca002
sio:SIO_000628
miriam-gene:6794
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_provenance
{
dgn-np:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_assertion
dcterms:description
"[Because intestinal carcinomas have been observed to develop in association with PJS, we analyzed tumors from 71 patients for allelic deletions (loss of heterozygosity) and STK11 gene mutations, to elucidate the etiological role of STK11 gene in sporadic colorectal cancer.]. 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:9809980
;
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:NP631494.RAptJn4_nIWMcLQKQegnXQjw0ngsdFH81ng5AqXAriyug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:21+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" .
}