@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc
> .
@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:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_head
{
this:
np:hasAssertion
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_assertion
a
np:Assertion
.
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_provenance
a
np:Provenance
.
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:675
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN149bca07bf44984f830b83af1fa2314c
sio:SIO_000628
miriam-gene:675
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_provenance
{
dgn-np:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_assertion
dcterms:description
"[In this article, we review the history of testing for mutations in breast cancer susceptibility genes and discuss the current state of testing for mutations in BRCA1 and BRCA2 in different clinical settings including at-risk individuals and cancer patients.]. 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:10819532
;
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:NP284518.RAJQZB1nkAYvJ3LLgJ9Tga_S6XYiAqshjq9Q--cpB6QCc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:54+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: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" .
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pav:version
"v4.0.0" .
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