@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_head
{
this:
np:hasAssertion
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_assertion
;
np:hasProvenance
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_assertion
a
np:Assertion
.
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_provenance
a
np:Provenance
.
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_assertion
{
miriam-gene:3046
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGNb62ef332d941071f1ea3715f198e0fac
sio:SIO_000628
miriam-gene:3046
,
lld:C0039730
;
a
sio:SIO_001122
.
}
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_provenance
{
dgn-np:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_assertion
dcterms: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]. 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-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP50225.RAWmruRAtpkfbEvu67cSJnVpy03BZLurg9iLboYnIFuXE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:07+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}