@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0
> .
@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:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_head
{
this:
np:hasAssertion
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_assertion
;
np:hasProvenance
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_assertion
a
np:Assertion
.
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_provenance
a
np:Provenance
.
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNace72f909f90364a7c2156fe73bc1c88
sio:SIO_000628
miriam-gene:5226
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_provenance
{
dgn-np:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_assertion
dcterms:description
"[PB-based approach has presently been utilized in PGD for genetic and chromosomal disorders, applied either separately, or together with embryo biopsy approaches, especially if there are two or more PGD indications.]. 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:21320873
;
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:NP418908.RAmgZm7jp42HASV_eRStH9kbiOsd3kfyHSPkkGirL2JV0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}