@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4
> .
@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:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_head
{
this:
np:hasAssertion
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_assertion
;
np:hasProvenance
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_provenance
;
np:hasPublicationInfo
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_assertion
a
np:Assertion
.
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_provenance
a
np:Provenance
.
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_assertion
{
miriam-gene:6490
a
ncit:C16612
.
lld:C1334177
a
ncit:C7057
.
dgn-gda:DGN813874ce992634e76990f3fa896a4376
sio:SIO_000628
miriam-gene:6490
,
lld:C1334177
;
a
sio:SIO_001121
.
}
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_provenance
{
dgn-np:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_assertion
dcterms:description
"[To test the prevalence of p53 polymorphism at codon 72 in 133 healthy women, 50 patients suffering from squamous intraepithelial lesions of the cervix (SIL), and 105 patients with invasive cervical cancer, we developed a polymerase chain reaction (PCR) and microtiter plate-based hybridisation assay.]. 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:11072671
;
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:NP800898.RAdFCLt0eglUHGwMt-XQm7idmvnDhwJ8dqXEY80yZaGo4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}