@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps
> .
@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:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_head
{
this:
np:hasAssertion
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_assertion
;
np:hasProvenance
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_provenance
;
np:hasPublicationInfo
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_assertion
a
np:Assertion
.
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_provenance
a
np:Provenance
.
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_assertion
{
miriam-gene:27030
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNda32a8a154e60234f311a90471901506
sio:SIO_000628
miriam-gene:27030
,
lld:C1140680
;
a
sio:SIO_001122
.
}
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_provenance
{
dgn-np:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_assertion
dcterms:description
"[We examined associations between 44 variants that tag the known common variants (minor allele frequency 0.05) in seven MMR genes (MLH1, MLH3, MSH2, MSH3, MSH6, PMS1 and PMS2) and survival of invasive ovarian cancer patients in three case-control studies from United Kingdom (UK), Denmark and California of United States of America (USA).]. 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:18723338
;
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:NP69834.RAXDU1Zp6Hh0pzNgtkHtqQFdjyoPxUaEAMKgvSUSxr-Ps130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}