@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g
> .
@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:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_head
{
this:
np:hasAssertion
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_assertion
;
np:hasProvenance
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_assertion
a
np:Assertion
.
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_provenance
a
np:Provenance
.
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGNf066907a4294a1aa22bd43cad2d95640
sio:SIO_000628
miriam-gene:2908
,
lld:C0007103
;
a
sio:SIO_001121
.
}
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_provenance
{
dgn-np:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_assertion
dcterms:description
"[The aim of this study was to evaluate the efficiency of the 'genotype restricted likelihood' (GRL) method that provides unbiased estimates of risks whatever the ascertainment process of families, and to estimate CRC and endometrial cancer risk for carriers of the MMR genes.]. 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:17473834
;
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:NP478959.RAdPFO1b-LoO0VNMJctiTzBDZIgzpgbQOvASKsSPNkT_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}