@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_assertion
;
np:hasProvenance
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_provenance
;
np:hasPublicationInfo
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_assertion
a
np:Assertion
.
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_provenance
a
np:Provenance
.
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:571
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGN04672cb262f24c104bb1d9f9f9ebbe3d
sio:SIO_000628
miriam-gene:571
,
lld:C0346153
;
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.
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dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_provenance
{
dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_assertion
dcterms:description
"[Together with previous studies, our results also indicate that although some rare germ line variants in BACH1 may contribute to breast cancer development, the contribution of BACH1 germline alterations to familial breast cancer seems marginal.]. 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:16430786
;
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 .
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dgn-np:NP168405.RAegM-DeypKytekfOMYx4Zqav9odILsk_bjCbJ4IvH8ZM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
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