@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho
> .
@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:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_head
{
this:
np:hasAssertion
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion
;
np:hasProvenance
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance
;
np:hasPublicationInfo
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion
a
np:Assertion
.
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance
a
np:Provenance
.
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN9f1a2f687a1ac8f664496660d0252c31
sio:SIO_000628
miriam-gene:672
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance
{
dgn-np:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion
dcterms:description
"[To determine whether there are any molecular markers that might help explain this paradox between pathologically aggressive neoplasms in patients with HBC and the lack of extreme clinically aggressive disease, we studied several molecular parameters in a group of 34 breast cancer patients with mutations in either the BRCA1 or BRCA2 tumor suppressor genes and compared them with a group of 20 breast cancer patients with non-HBC.]. 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:9781655
;
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:NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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
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"v2.1.0" .
}