@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA
> .
@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:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_head
{
this:
np:hasAssertion
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_assertion
;
np:hasProvenance
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_provenance
;
np:hasPublicationInfo
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_assertion
a
np:Assertion
.
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_provenance
a
np:Provenance
.
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN4dc228579f9eaec4928df2ef65635c5d
sio:SIO_000628
miriam-gene:26227
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_provenance
{
dgn-np:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_assertion
dcterms:description
"[Preimplantation genetic diagnosis (PGD) has been suggested as an alternative by which asymptomatic individuals who are at high risk of carrying HD can avail themselves of antenatal genetic testing without incurring the emotional, social and financial burdens that might result from the presymptomatic disclosure of their own carrier status.]. 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:9949442
;
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:NP526926.RAQ34Sy4TvfBTsoGXpZbazOZdF8vL1ipV9323Jb1taQBA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:16+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" .
}