@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s
> .
@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:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_head
{
this:
np:hasAssertion
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_assertion
;
np:hasProvenance
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_assertion
a
np:Assertion
.
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_provenance
a
np:Provenance
.
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C2919828
a
ncit:C7057
.
dgn-gda:DGNdd627502f3c24f142ff353585a41f96a
sio:SIO_000628
miriam-gene:7157
,
lld:C2919828
;
a
sio:SIO_001121
.
}
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_provenance
{
dgn-np:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_assertion
dcterms:description
"[We have examined the frequency of allelic loss of the p53 gene in carcinoma and dysplasia arising in patients with chronic ulcerative colitis who are heterozygous for the codon 72 polymorphism in exon 4 of the p53 gene.]. 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:2049225
;
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:NP801740.RA2JVNg0RLqpjU2-Notw2lTbihfAh0Ulv3VPdEy2yxH9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}