@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs
> .
@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:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_head
{
this:
np:hasAssertion
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion
;
np:hasProvenance
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance
;
np:hasPublicationInfo
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion
a
np:Assertion
.
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance
a
np:Provenance
.
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion
{
miriam-gene:4830
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGNc821e3511338afaa5308596eec263077
sio:SIO_000628
miriam-gene:4830
,
lld:C0014170
;
a
sio:SIO_001122
.
}
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_provenance
{
dgn-np:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_assertion
dcterms:description
"[Heterozygous genotypes TC in rs16949649 and CT in rs2302254 of nm23-H1 promoter are potential susceptibility factors for endometrial cancer in Taiwan women. Once having the endometrial cancer, Taiwan women with variant homozygote CC in rs1694964 were at less risk to have non-endometrioid type, while women with variant homozygote TT in rs2302254 tended to have advanced stage 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:20599259
;
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:NP83837.RAGNA87KU0cfMs3MbjENOsPQxTNydQFvXHDo_jGtslXNs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:41+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" .
}