@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw
> .
@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:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_head
{
this:
np:hasAssertion
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion
;
np:hasProvenance
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance
;
np:hasPublicationInfo
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion
a
np:Assertion
.
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance
a
np:Provenance
.
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion
{
miriam-gene:6236
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGNf10b62936c05578cbf22807896deafc3
sio:SIO_000628
miriam-gene:6236
,
lld:C0039730
;
a
sio:SIO_001121
.
}
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_provenance
{
dgn-np:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_assertion
dcterms:description
"[A retrospective study was performed to compare the detection rate of chromosomal abnormalities by different approaches of full karyotyping, rapid aneuploidy diagnosis (RAD) or both when invasive prenatal testing is performed for diagnosis of thalassaemia.]. 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:16421217
;
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:NP405941.RApMen19XSPTj0SzLpsMX3oMNh9piBVbmi2wKV6l4-tIw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}