@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU
> .
@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:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_head
{
this:
np:hasAssertion
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion
;
np:hasProvenance
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance
;
np:hasPublicationInfo
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion
a
np:Assertion
.
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance
a
np:Provenance
.
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0085183
a
ncit:C7057
.
dgn-gda:DGNc46d2c0f1f32d71fb3a10f38ccd4fe62
sio:SIO_000628
miriam-gene:672
,
lld:C0085183
;
a
sio:SIO_001121
.
}
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_provenance
{
dgn-np:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_assertion
dcterms:description
"[As such, their identification is essential to reduce the risk of disease in healthy carriers, as well as in carriers who have already developed the disease because they are at increased risk for a second malignancy; moreover, noncarriers of BRCA1 and BRCA2 mutated families can be spared anxiety and unnecessary medical interventions.]. 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:11920643
;
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:NP668738.RAofIEvFyUo1-OHAfScsPd_92RYK37vh-qo1-Gc0-N1VU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}