@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck
> .
@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:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_head
{
this:
np:hasAssertion
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_assertion
;
np:hasProvenance
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_provenance
;
np:hasPublicationInfo
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_assertion
a
np:Assertion
.
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_provenance
a
np:Provenance
.
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN8648c2ecd92281bcdaca6dada8b9d708
sio:SIO_000628
miriam-gene:26227
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_provenance
{
dgn-np:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_assertion
dcterms:description
"[To perform a cost-benefit analysis of preimplantation genetic diagnosis (PGD) for carrier couples of cystic fibrosis (CF) compared with the alternative of natural conception (NC) followed by prenatal testing and termination of affected pregnancies.]. 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:19439290
;
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:NP318774.RAXdHRk8E-9cjTF1BRlbq3MnAg8fuUAss5efj3DDg25Ck130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}