@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc
> .
@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:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_head
{
this:
np:hasAssertion
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_assertion
;
np:hasProvenance
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_provenance
;
np:hasPublicationInfo
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_assertion
a
np:Assertion
.
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_provenance
a
np:Provenance
.
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_assertion
{
miriam-gene:1012
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGN4a8d009b193e01830e8587df67631aba
sio:SIO_000628
miriam-gene:1012
,
lld:C0007103
;
a
sio:SIO_001121
.
}
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_provenance
{
dgn-np:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_assertion
dcterms:description
"[We investigated DNA isolated from vaginal secretion collected from tampon for aberrant methylation of five genes (CDH13, HSPA2, MLH1, RASSF1A, and SOCS2) using MethyLight in 15 patients with endometrial cancer and 109 patients without endometrial 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:15159323
;
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:NP818065.RAjnE7An6mkEgcZKxg30GTzcGnDQFlLnxjEHIGosx73mc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}