@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE
> .
@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:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_head
{
this:
np:hasAssertion
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_assertion
;
np:hasProvenance
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_provenance
;
np:hasPublicationInfo
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_assertion
a
np:Assertion
.
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_provenance
a
np:Provenance
.
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0036323
a
ncit:C7057
.
dgn-gda:DGN7bc0a097c54bb5fed33e85ff2aeb8806
sio:SIO_000628
miriam-gene:7157
,
lld:C0036323
;
a
sio:SIO_001121
.
}
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_provenance
{
dgn-np:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_assertion
dcterms:description
"[To shed light on the mechanisms underlying these different patterns of bladder cancer we looked for mutations in the p53 gene in SBC from 92 patients in Egypt, where schistosomiasis is hyperendemic.]. 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:7767983
;
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:NP895228.RAE5XC9w5PwJAenflbRYnBWVQ1dE4KQ5Ex9k5mE0dsLeE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}