@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA
> .
@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:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_head
{
this:
np:hasAssertion
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_assertion
a
np:Assertion
.
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_provenance
a
np:Provenance
.
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN6864c995b7efe4e0e9becf9f165257a8
sio:SIO_000628
miriam-gene:672
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_provenance
{
dgn-np:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_assertion
dcterms:description
"[Altogether our results suggest that HBC families, the largest pool in our series, represent an heterogeneous group where the apparently faulty performances of the prediction models might be at least partially explained by the presence of additional kinds of BRCA1/2 alteration (such as genomic rearrangements) or by mutations on different breast cancer related genes.]. 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:16760289
;
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:NP553561.RAKVDRJ5PtxSvlsYHzvUwwkjUXF-em6GuTAgKRmRPDExA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:55+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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"v4.0.0" .
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