@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q
> .
@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:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_head
{
this:
np:hasAssertion
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_assertion
;
np:hasProvenance
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_assertion
a
np:Assertion
.
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_provenance
a
np:Provenance
.
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN1847afa0b61597e4181d874b93cb2f25
sio:SIO_000628
miriam-gene:675
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_provenance
{
dgn-np:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_assertion
dcterms:description
"[Risk assessment, genetic counseling, and BRCA1/BRCA2 mutation testing, especially for younger women with breast cancer, have started to be an integral element of practice due to advances in gene sequencing technologies and accumulating evidence for the clinical implications of BRCA mutation status for not only early breast cancer management, but also for the patient's own and their family's next cancer risk, and proactive steps toward a risk-reducing approach.]. 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:23754181
;
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:NP1084779.RAQ36bJdqbJm7TpTERbsjFySncBSsQ1qvpxqO7DOdTI7Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:57+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" .
}