@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s
> .
@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 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:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_head
{
this:
np:hasAssertion
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_assertion
;
np:hasProvenance
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_assertion
a
np:Assertion
.
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_provenance
a
np:Provenance
.
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_assertion
{
miriam-gene:3039
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGNacec72c5d164ea61dfeb10b5f8147414
sio:SIO_000628
miriam-gene:3039
,
lld:C0039730
;
a
sio:SIO_001122
.
}
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_provenance
{
dgn-np:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_assertion
dct:description
"[ Based on the above figures and known prevalence rates of thalassaemia carriers, it would seem worthwhile to screen for globin gene mutations in partners of known thalassaemia carriers, regardless of MCV, to identify pregnancies at risk of Hb H disease or Hb E/beta thalassaemia.]. 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:11304851
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP42676.RArDMbjVGWUGivejE8ekUyli1i5wivMMDbY0KGNPgrZ0s130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}