@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE
> .
@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:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_head
{
this:
np:hasAssertion
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_assertion
;
np:hasProvenance
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_assertion
a
np:Assertion
.
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_provenance
a
np:Provenance
.
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNb3d1cb140b603a2e354f039d34882028
sio:SIO_000628
miriam-gene:672
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_provenance
{
dgn-np:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_assertion
dcterms:description
"[In this study, we performed a screening of BRCA1 and BRCA2 in families from northern Italy with familial recurrence of breast cancer or ovarian cancer in which the individual risk of patients of being carriers of BRCA1 and BRCA2 mutation was evaluated using BRCAPRO (CAGene) software.]. 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:21042765
;
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:NP308627.RAgPbAwhFAI6-Mfnd17IpGgWRfJTrwMT8QGk3D1J0JWWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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: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" .
}