@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c
> .
@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:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_head
{
this:
np:hasAssertion
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_assertion
;
np:hasProvenance
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_assertion
a
np:Assertion
.
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_provenance
a
np:Provenance
.
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C2986662
a
ncit:C7057
.
dgn-gda:DGN732ef79e447cc1fb4509509b6785e0a0
sio:SIO_000628
miriam-gene:672
,
lld:C2986662
;
a
sio:SIO_001121
.
}
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_provenance
{
dgn-np:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_assertion
dcterms:description
"[To estimate the prevalence and spectrum of BRCA1 and BRCA2 mutations in young Danish patients affected with bilateral or multifocal breast cancer and to determine the relationship of mutation status to 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:11389159
;
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:NP185118.RADQOZ0TkidXXSD4TRTuQgGujP8_8YV1lz4pZRYqxiV_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}