@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk
> .
@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:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_head
{
this:
np:hasAssertion
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_assertion
;
np:hasProvenance
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_provenance
;
np:hasPublicationInfo
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_assertion
a
np:Assertion
.
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_provenance
a
np:Provenance
.
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0751483
a
ncit:C7057
.
dgn-gda:DGN6af33b4d6a79901f63439d0d6295ec6b
sio:SIO_000628
miriam-gene:26227
,
lld:C0751483
;
a
sio:SIO_001121
.
}
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_provenance
{
dgn-np:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_assertion
dcterms:description
"[This paper reports the first clinical experience of preimplantation genetic diagnosis (PGD) for hereditary retinoblastoma using two highly polymorphic microsatellite markers RB1.20 and D13S284, located within and close to the RB1 gene respectively.]. 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:12569181
;
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:NP412542.RA5Uk7BvkyXxSyLnliX0w9T2zI9mvsX6ENeinSYEcmhzk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}