@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c
> .
@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:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_head
{
this:
np:hasAssertion
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_assertion
;
np:hasProvenance
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_assertion
a
np:Assertion
.
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_provenance
a
np:Provenance
.
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_assertion
{
miriam-gene:4535
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN23ac73704f5774d459e2f39a212fd002
sio:SIO_000628
miriam-gene:4535
,
lld:C0476089
;
a
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.
}
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_provenance
{
dgn-np:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_assertion
dcterms:description
"[To investigate the relationship between mtDNA variation and endometrial cancer, we collected blood samples from subjects with Han native background in Yunnan province in China, 49 of them with pathologically conformed endometrial cancer and 31 as controls with no cancer disease and sequenced two hypervariable segments of control region, part of 16sRNA gene, tRNA(leu) (tRNA is transfer RNA) gene and ND1 gene of mtDNA and identified some diagnostic polymorphisms by restriction fragment length polymorphism of coding region of mtDNA.]. 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:16884381
;
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:NP824712.RAnny_cBieZbFBRX-s4jyPb0vCR7_ov5HO7qCmvK6Pj1c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}