@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA
> .
@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:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_head
{
this:
np:hasAssertion
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_assertion
;
np:hasProvenance
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_assertion
a
np:Assertion
.
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_provenance
a
np:Provenance
.
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN5026b899fc16811bfcda4c1cbcc4b7b4
sio:SIO_000628
miriam-gene:4360
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_provenance
{
dgn-np:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_assertion
dcterms:description
"[To understand the mechanisms regulating the transition from indolent to invasive disease, we profiled somatic copy number alterations in noninvasive adenomas and invasive adenocarcinomas from Apc and DNA mismatch repair (MMR) mutant mouse models.]. 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:22628407
;
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:NP677622.RA6LSSnAlVs1D_pePMxbckefMoG6ml5p4ddPuq24dyMAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}