@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA
> .
@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:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_head
{
this:
np:hasAssertion
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_assertion
;
np:hasProvenance
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_assertion
a
np:Assertion
.
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_provenance
a
np:Provenance
.
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_assertion
{
miriam-gene:9338
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGNb23d61f758131b708c89e2f4224712c8
sio:SIO_000628
miriam-gene:9338
,
lld:C0302592
;
a
sio:SIO_001122
.
}
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_provenance
{
dgn-np:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_assertion
dcterms:description
"[We compared the distribution of the p21 genotype in ICC, CIN III, and control and also analyzed the association of this polymorphism with the risk of development of cervical cancer, especially in patients with high-risk human papillomavirus (HPV) (16 or 18)-positive 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:11248419
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP50806.RASMDo-vLRW8tO1_PGEtvtfeNa8oF_w_X73qbso6-AIfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}