@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI
> .
@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:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_head
{
this:
np:hasAssertion
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_assertion
;
np:hasProvenance
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_provenance
;
np:hasPublicationInfo
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_assertion
a
np:Assertion
.
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_provenance
a
np:Provenance
.
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGN05da61d5f8a0c31b9e5a95e917f1ed5b
sio:SIO_000628
miriam-gene:26227
,
lld:C0039730
;
a
sio:SIO_001121
.
}
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_provenance
{
dgn-np:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_assertion
dcterms:description
"[Haemoglobin disorders are among the most frequent indications for preimplantation genetic diagnosis (PGD), introduced as an important option to couples at risk for producing offspring with thalassaemia and sickle cell disease.]. 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:16176679
;
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:NP453861.RA507PPbZ4AfWwhMPB7eRaNqogB6DBnUG3YT7RY8oUzbI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}