@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ
> .
@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:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_head
{
this:
np:hasAssertion
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_assertion
;
np:hasProvenance
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_assertion
a
np:Assertion
.
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_provenance
a
np:Provenance
.
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0349458
a
ncit:C7057
.
dgn-gda:DGNd2f0f6a0ff17ef996242ecdc0af46d63
sio:SIO_000628
miriam-gene:2272
,
lld:C0349458
;
a
sio:SIO_001121
.
}
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_provenance
{
dgn-np:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_assertion
dcterms:description
"[The presence of high-risk human papillomavirus, loss of heterozygosity on chromosome 3p and fragile histidine triad gene expression were assessed as potential markers of cancer and CIN progression in 83 cervical cancers and 74 cervical intraepithelial neoplasia grade 1 lesions.]. 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:15570308
;
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:NP849884.RA83juGZdMWmhpRCfQQGhNc4bkGFLhCAAmHX_gBrgrqSQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}