@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0
> .
@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:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_head
{
this:
np:hasAssertion
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_assertion
;
np:hasProvenance
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_provenance
;
np:hasPublicationInfo
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_assertion
a
np:Assertion
.
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_provenance
a
np:Provenance
.
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0376415
a
ncit:C7057
.
dgn-gda:DGN3a7f0055086188de7bcc5b56bbac5f93
sio:SIO_000628
miriam-gene:5226
,
lld:C0376415
;
a
sio:SIO_001121
.
}
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_provenance
{
dgn-np:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_assertion
dcterms:description
"[Preimplantation genetic diagnosis (PGD) has recently been performed for inherited cancer predisposition determined by p53 tumour suppressor gene mutations, suggesting the usefulness of PGD for late onset disorders with genetic predisposition, including those caused by the germline mutations of other tumour suppressor genes.]. 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:12709270
;
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:NP864922.RAyNBF04usbV7oPk6UxE_6vIm6VK6xrB-FscjxAml-cu0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}