@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA
> .
@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:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_head
{
this:
np:hasAssertion
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_assertion
;
np:hasProvenance
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_assertion
a
np:Assertion
.
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_provenance
a
np:Provenance
.
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN06e0a3d7d91c37290e625eff952410a9
sio:SIO_000628
miriam-gene:1565
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_provenance
{
dgn-np:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_assertion
dcterms:description
"[Whereas, frequency distribution for the same combination between severe dysplasia and squamous cell carcinoma failed to attain any statistical significance suggesting that CIN III with CYP2D6 EM genotype has less chance to progress to cervical cancer.]. 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:19356055
;
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:NP161876.RAIBnHhvSyn-xxGoPYvn_wj31rXTCEGk4lgCBKrpdedaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}