@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk
> .
@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:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_head
{
this:
np:hasAssertion
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_assertion
;
np:hasProvenance
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_provenance
;
np:hasPublicationInfo
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_assertion
a
np:Assertion
.
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_provenance
a
np:Provenance
.
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_assertion
{
miriam-gene:6223
a
ncit:C16612
.
lld:C0005283
a
ncit:C7057
.
dgn-gda:DGN7bbae9a2b5e9a981df5e4267a58dd514
sio:SIO_000628
miriam-gene:6223
,
lld:C0005283
;
a
sio:SIO_001121
.
}
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_provenance
{
dgn-np:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_assertion
dcterms:description
"[These include globin gene switching in alpha and beta thalassemia, the expression of red cell antigens in alloimmune hemolytic disease, and the poorly understood defects in the regulation of erythropoiesis in Diamond Blackfan anemia.]. 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:9661799
;
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:NP407429.RAahOi8_ojRqUxXaIlgOk7CUe8zdUtpQc4_rBJcLn8xGk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}