@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo
> .
@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:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_head
{
this:
np:hasAssertion
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion
;
np:hasProvenance
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance
;
np:hasPublicationInfo
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion
a
np:Assertion
.
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance
a
np:Provenance
.
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN545fd20ce163bc7a82b4e5d4dab33713
sio:SIO_000628
miriam-gene:54658
,
lld:C0476089
;
a
sio:SIO_001122
.
}
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance
{
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion
dcterms:description
"[These findings define those populations with a high frequency of hemoglobin E-beta-thalassemia and related disorders that are at increased risk for hyperbilirubinemia and gall bladder disease and provide evolutionary insights into how these polymorphisms have arisen and are so unequally distributed among human populations.]. 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:12850492
;
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:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}