@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0
> .
@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:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_head
{
this:
np:hasAssertion
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_assertion
;
np:hasProvenance
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_provenance
;
np:hasPublicationInfo
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_assertion
a
np:Assertion
.
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_provenance
a
np:Provenance
.
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0281267
a
ncit:C7057
.
dgn-gda:DGN3c498b6ac3d79e80c5439f1abddcbc6a
sio:SIO_000628
miriam-gene:672
,
lld:C0281267
;
a
sio:SIO_001121
.
}
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_provenance
{
dgn-np:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_assertion
dcterms:description
"[It was shown that the presence of the mutations in the BRCA1/2 genes among patients with bilateral breast cancer is associated with an earlier occurrence of the first and the second breast cancer than in patients without hereditary mutations in these genes (a difference of 7.2-8.4 years).]. 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:19372713
;
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:NP482782.RAFjaZeanlwV25o2rOaFEG3xpgmUnOa4HiTxQaPmJP7D0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}