@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ
> .
@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:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_head
{
this:
np:hasAssertion
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_assertion
;
np:hasProvenance
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_assertion
a
np:Assertion
.
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_provenance
a
np:Provenance
.
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0037176
a
ncit:C7057
.
dgn-gda:DGNfc9f46a9ddae729f7ea4b476045a049e
sio:SIO_000628
miriam-gene:26227
,
lld:C0037176
;
a
sio:SIO_001121
.
}
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_provenance
{
dgn-np:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_assertion
dcterms:description
"[Preimplantation genetic diagnosis (PGD) of single gene defects following assisted conception typically involves removal of single cells from preimplantation embryos and analysis using highly sensitive PCR amplification methods taking stringent precautions to prevent contamination from foreign or previously amplified DNA.]. 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:15322224
;
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:NP719854.RAI6sLow3XQyV8jIe7wE3GzeGHqAlUiR7WVDNUE_5MYxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}