@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag
> .
@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:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_head
{
this:
np:hasAssertion
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_assertion
;
np:hasProvenance
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_provenance
;
np:hasPublicationInfo
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_assertion
a
np:Assertion
.
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_provenance
a
np:Provenance
.
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0345905
a
ncit:C7057
.
dgn-gda:DGN7d2983ebb3ba8385fea66e010b0c1551
sio:SIO_000628
miriam-gene:7157
,
lld:C0345905
;
a
sio:SIO_001121
.
}
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_provenance
{
dgn-np:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_assertion
dcterms:description
"[Extension of this analysis to the use of ICC on 104 colonic lesions, representative of different stages of colonic neoplastic progression, showed an absence of detectable p53 nuclear staining in preneoplastic polyp lesions (20 cases) with staining of 52% (25/48) of primary colon carcinomas and 81% (29/36) of hepatic metastases, suggestive of an increased incidence of p53 mutations in late stage lesions of colonic 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:7651727
;
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:NP446693.RA9KevwT8ngoCvyK9Bn1u-lKSwBN1CBSB0f06euFgP_Ag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}