@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M
> .
@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:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_head
{
this:
np:hasAssertion
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_assertion
;
np:hasProvenance
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_provenance
;
np:hasPublicationInfo
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_assertion
a
np:Assertion
.
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_provenance
a
np:Provenance
.
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNbcdf39eee444b1c9e7cbaa2d957ee4d0
sio:SIO_000628
miriam-gene:5226
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_provenance
{
dgn-np:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_assertion
dcterms:description
"[A review of the most common infertility-associated chromosomal and genetic diseases for which genetic testing has become routine in infertile parents and in the products of assisted reproduction through preimplantation genetic diagnosis (PGD) and prenatal testing follows.]. 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:10913952
;
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:NP337512.RAEU0mtxpf31-fy9NaBFUhq_24eFEwzNZayLVzTpbQy0M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}