@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw
> .
@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:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_head
{
this:
np:hasAssertion
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_assertion
;
np:hasProvenance
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_provenance
;
np:hasPublicationInfo
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_assertion
a
np:Assertion
.
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_provenance
a
np:Provenance
.
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_assertion
{
miriam-gene:4536
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN9aba404dee4d5834b44e8656db2ce4fd
sio:SIO_000628
miriam-gene:4536
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_provenance
{
dgn-np:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_assertion
dcterms:description
"[After applying three Cox proportional hazard models adjusted for American Joint Committee on Cancer (AJCC) stage, age and sex, three single nucleotide polymorphisms, two located in the 12S ribosomal RNA region (G752A and G1440A) and one in the nicotinamide adenine dinucleotide dehydrogenase subunit 2 region (ND2) region (G4770A), were statistically significantly associated with all-cause (Model I P-values: 0.0001, 0.002 and 0.002, respectively) and CRC-specific mortality (Model I P-values: 5 x 10(-5), 0.0003 and 0.0006, respectively).]. 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:19945968
;
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:NP870930.RAFRzvGhctgEJlSA3K12-cqMKyq42HnxdK_jcGqbHmdEw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}