@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_assertion
;
np:hasProvenance
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_provenance
;
np:hasPublicationInfo
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_assertion
a
np:Assertion
.
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_provenance
a
np:Provenance
.
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_assertion
{
miriam-gene:84168
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN4426f26eeaa9f8681e6027af00abb674
sio:SIO_000628
miriam-gene:84168
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_provenance
{
dgn-np:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_assertion
dcterms:description
"[We conclude that common alleles of ATR and CHEK1 are not implicated in breast cancer risk or survival, but we cannot exclude effects of rare alleles and of common alleles with very small effect sizes.]. 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:23844225
;
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:NP461663.RA7nIJRdj6lWg86smgbFlFaY0J2TJ4bXdW58opSZJk7n8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}