@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_head
{
this:
np:hasAssertion
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_assertion
;
np:hasProvenance
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_assertion
a
np:Assertion
.
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_provenance
a
np:Provenance
.
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN5708030c2522db2906fdee1539b1aac0
sio:SIO_000628
miriam-gene:675
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_provenance
{
dgn-np:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_assertion
dcterms:description
"[Five cases carried the BRCA1 C4446T mutation and two cases carried the BRCA2 8765delAG mutation which are the most common mutations that have been described in French Canadian breast cancer and breast ovarian cancer families.]. 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:10422801
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP258699.RA0EJii1FFK1nzBuTa1G3FtCcQoT3a29ahHs4k3u9cWLQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:43+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}