@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w
> .
@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:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_head
{
this:
np:hasAssertion
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_assertion
;
np:hasProvenance
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_provenance
;
np:hasPublicationInfo
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_assertion
a
np:Assertion
.
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_provenance
a
np:Provenance
.
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_assertion
{
miriam-gene:26227
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGN0d9ca2aa3bf35de3e339d7b90a19228f
sio:SIO_000628
miriam-gene:26227
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_provenance
{
dgn-np:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_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:NP641030.RA8p560JIedHHj1zS5AS6PozGCq1hErJr0oZCTJAXuj6w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}