@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo
> .
@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:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_head
{
this:
np:hasAssertion
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_assertion
;
np:hasProvenance
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_provenance
;
np:hasPublicationInfo
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_assertion
a
np:Assertion
.
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_provenance
a
np:Provenance
.
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNba1d49eb8fae21502133abd6b4d872b6
sio:SIO_000628
miriam-gene:5226
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_provenance
{
dgn-np:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_assertion
dcterms:description
"[Clinical applications of this assay should enable detection of those embryos that have inherited three heterozygous alleles and, therefore, benefit many PGD patients who are at an increased risk of Down's syndrome.]. 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:10587373
;
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:NP787706.RA0Tj73KsNBXeFDBT6LWAF7K_ZArMeDa_5DH-xkzLW3Vo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}