@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI
> .
@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:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_head
{
this:
np:hasAssertion
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_assertion
;
np:hasProvenance
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_provenance
;
np:hasPublicationInfo
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_assertion
a
np:Assertion
.
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_provenance
a
np:Provenance
.
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0281267
a
ncit:C7057
.
dgn-gda:DGNca480a9ab23bc6896f7f730e2867405e
sio:SIO_000628
miriam-gene:11200
,
lld:C0281267
;
a
sio:SIO_001121
.
}
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_provenance
{
dgn-np:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_assertion
dcterms:description
"[Our research focused on the relations between the age at onset of bilateral breast cancer and the prevalence of selected hereditary BRCA1, BRCA2 and CHEK2 gene mutations with reference to their positive family history of cancer.]. 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:NP783353.RAHRwAz4VR2T1GxMvRLzkRmCJeinlKV4huyOuCVXXnLVI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}