@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs
> .
@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:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_head
{
this:
np:hasAssertion
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_assertion
;
np:hasProvenance
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_provenance
;
np:hasPublicationInfo
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_assertion
a
np:Assertion
.
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_provenance
a
np:Provenance
.
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0677776
a
ncit:C7057
.
dgn-gda:DGNe94b4584539ba02d3cd7af41e3fdcbd4
sio:SIO_000628
miriam-gene:5226
,
lld:C0677776
;
a
sio:SIO_001121
.
}
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_provenance
{
dgn-np:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_assertion
dcterms:description
"[In May 2006, the UK Human Fertilization and Embryology Authority (HFEA) approved use of preimplantation genetic diagnosis (PGD) for lower penetrance, late onset cancer susceptibility syndromes such as hereditary breast and ovarian cancer (HBOC).]. 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:17428877
;
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:NP824876.RAGBlwRku8FrsQYtmcfCVT6IonaS8aqQ7nWdWMCAopbrs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}