@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo
> .
@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:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_head
{
this:
np:hasAssertion
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_assertion
;
np:hasProvenance
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_provenance
;
np:hasPublicationInfo
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_assertion
a
np:Assertion
.
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_provenance
a
np:Provenance
.
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN7fdf1f4b81e8e1f541cc4a7681f2a341
sio:SIO_000628
miriam-gene:26227
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_provenance
{
dgn-np:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_assertion
dcterms:description
"[Novel indications for PGD not readily applicable by traditional prenatal genetic diagnosis include avoiding clinical pregnancy termination, performing preconceptional diagnosis (polar body I), obtaining prenatal diagnosis without disclosure of prenatal genotype (nondisclosure), diagnosing adult-onset disorders particularly cancer, and identifying HLA compatible embryos suitable for recovering umbilical cord blood stem cells.]. 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:20572111
;
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:NP532060.RAQuK7V5UKohN-S1mg7w26ofx9Hbm72onCVuRWNZ82Aoo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}