@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g
> .
@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:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_head
{
this:
np:hasAssertion
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion
;
np:hasProvenance
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion
a
np:Assertion
.
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance
a
np:Provenance
.
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion
{
miriam-gene:5242
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN4074b10c9a9e436280cd5c847a45a7e1
sio:SIO_000628
miriam-gene:5242
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance
{
dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion
dcterms:description
"[To compare the incidence of chromosomal abnormalities in preimplantation embryos from couples undergoing preimplantation genetic screening (PGS) after previous aneuploid miscarriage after either natural conception (NC) or assisted reproductive technology (ART) versus fertile couples who underwent PGS for sex-linked diseases as a control group.]. 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:22521156
;
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:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}