@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY
> .
@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:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_head
{
this:
np:hasAssertion
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_assertion
;
np:hasProvenance
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_provenance
;
np:hasPublicationInfo
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_assertion
a
np:Assertion
.
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_provenance
a
np:Provenance
.
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_assertion
{
miriam-gene:5669
a
ncit:C16612
.
lld:C0007847
a
ncit:C7057
.
dgn-gda:DGNbe77ead97ae0719bd8e9b5dec3cc305b
sio:SIO_000628
miriam-gene:5669
,
lld:C0007847
;
a
sio:SIO_001121
.
}
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_provenance
{
dgn-np:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_assertion
dcterms:description
"[Comparison of the two groups revealed that isolates from cervical cancers predominantly carry changes in sequences of YY1 binding sites (especially at nucleotide 7519), while variants from asymptomatic carriers contained nucleotide changes within or close to transcription binding sites for AP-1, Oct-1, NF1, Tef-1, Tef-2, Sp1, YY1 and viral E2.]. 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:11595585
;
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:NP599385.RAHx7DodrgSBDdL5vQ8sU9I_KQ1X4Ah55VI82WRyAk2lY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}