@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA
> .
@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:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_head
{
this:
np:hasAssertion
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion
;
np:hasProvenance
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance
;
np:hasPublicationInfo
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion
a
np:Assertion
.
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance
a
np:Provenance
.
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion
{
miriam-gene:55655
a
ncit:C16612
.
lld:C0281267
a
ncit:C7057
.
dgn-gda:DGN3a1b4e23fa9b1dbd0bf6d9afdeaa9eba
sio:SIO_000628
miriam-gene:55655
,
lld:C0281267
;
a
sio:SIO_001121
.
}
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_provenance
{
dgn-np:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_assertion
dcterms:description
"[Recent studies have demonstrated that heterozygous carriers of the NBS1 657del5 mutation have an increased risk for familial and bilateral breast cancer, but similar studies in consecutive breast cancer patients were inconclusive.]. 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:16770759
;
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:NP887831.RABZYU-_n_t5oG-vPwu2r4N_oRo1fu8JmGV7Q0orR4dYA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:05+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
pav:version
"v2.1.0" .
}