@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI
> .
@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:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_head
{
this:
np:hasAssertion
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_assertion
;
np:hasProvenance
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_provenance
;
np:hasPublicationInfo
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_assertion
a
np:Assertion
.
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_provenance
a
np:Provenance
.
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN61b935875a254719e0099a418518d4d4
sio:SIO_000628
miriam-gene:8170
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_provenance
{
dgn-np:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_assertion
dcterms:description
"[Our study shows that -26 5' UTR polymorphism in BRCA2 can modulate the fine-tuned regulation of the multifunctional gene BRCA2 and renders risk or protection according to the genotype status in the sporadic form of breast cancer, which is further influenced by the germline genetic backgrounds of codon 72 polymorphism of p53.]. 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:17945002
;
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:NP177374.RAYGsbttlQGbBSXq4wUJBuwe9gg6CHd9FBlSV3UyWS2fI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}