@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540
> .
@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:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_head
{
this:
np:hasAssertion
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_assertion
;
np:hasProvenance
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_provenance
;
np:hasPublicationInfo
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_assertion
a
np:Assertion
.
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_provenance
a
np:Provenance
.
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0033036
a
ncit:C7057
.
dgn-gda:DGNa1dee1c1d3bb0cf358f7216b6f4aa92f
sio:SIO_000628
miriam-gene:324
,
lld:C0033036
;
a
sio:SIO_001121
.
}
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_provenance
{
dgn-np:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_assertion
dcterms:description
"[In this study we set out to test the hypothesis that loss of Rassf1a can cooperate with inactivation of the adenomatous polyposis coli (Apc) gene to accelerate intestinal tumourigenesis using the Apc-Min (Apc(Min/+)) mouse model, as mutational or deletional inactivation of APC is a frequent early event in the genesis of intestinal 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:18391979
;
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:NP357807.RAt6kzRR0ltOs9xgvF0Pe7181HfurTq52sz5Ykw3en540130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}