@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo
> .
@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:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_head
{
this:
np:hasAssertion
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_assertion
;
np:hasProvenance
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_assertion
a
np:Assertion
.
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_provenance
a
np:Provenance
.
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_assertion
{
miriam-gene:3043
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGN3ca6dbffe2eb0e7b9c41ebe8013dd14a
sio:SIO_000628
miriam-gene:3043
,
lld:C0039730
;
a
sio:SIO_001121
.
}
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_provenance
{
dgn-np:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_assertion
dcterms:description
"[In this preliminary analysis of 587 bp of the HBB gene in selected thalassemic individuals, some rare mutations in world perspective have been found to be significantly high in the Bangladeshi population, together with the common mutations for thalassemia.]. 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:20406103
;
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:NP770379.RAzEQRmgrsH6CnbqYRGgmGbdqR7hGloIgU-O_c8IA4dRo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}