@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI
> .
@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:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_head
{
this:
np:hasAssertion
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_assertion
;
np:hasProvenance
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_provenance
;
np:hasPublicationInfo
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_assertion
a
np:Assertion
.
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_provenance
a
np:Provenance
.
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_assertion
{
miriam-gene:4089
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN2a754c198aad1eb9bbb93410413356a6
sio:SIO_000628
miriam-gene:4089
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_provenance
{
dgn-np:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_assertion
dcterms:description
"[Five specific chromosomal aberrations, combined with immunohistochemistry for p53 and SMAD4, can predict possible progression of sessile rectal adenomas to early rectal cancer and can, after validation studies, be added to preoperative staging.]. 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:18245538
;
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:NP592153.RAXxuDBVHDXrF22jkogXb5A76P-B_pWXsZ0nJWyvGIXBI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}