@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU
> .
@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:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_head
{
this:
np:hasAssertion
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion
;
np:hasProvenance
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance
;
np:hasPublicationInfo
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion
a
np:Assertion
.
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance
a
np:Provenance
.
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion
{
miriam-gene:8266
a
ncit:C16612
.
lld:C0017758
a
ncit:C7057
.
dgn-gda:DGN0b22f0ea5246bb24b428a96d96afd770
sio:SIO_000628
miriam-gene:8266
,
lld:C0017758
;
a
sio:SIO_001121
.
}
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance
{
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion
dcterms:description
"[The frequencies of four major red cell genetic defects, sickle haemoglobin (Hb S), glucose 6 phosphate dehydrogenase deficiency (G6PD), and alpha and beta thalassaemia, have been determined in nearly 5000 subjects from the three major Peninsular Arab States, namely Yemen (North and South), the United Arab Emirates, and Oman.]. 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:3723553
;
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:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}