@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y
> .
@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:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_head
{
this:
np:hasAssertion
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_assertion
;
np:hasProvenance
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_assertion
a
np:Assertion
.
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_provenance
a
np:Provenance
.
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGN70debc8ee19bb03c21286889fab3bde3
sio:SIO_000628
miriam-gene:2056
,
lld:C0039730
;
a
sio:SIO_001121
.
}
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_provenance
{
dgn-np:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_assertion
dcterms:description
"[There is also an emerging understanding that the HbE thalassemia phenotype may be unstable, which may reflect changes in adaptation to anemia and, possibly, attenuation of the erythropoietin response over time.]. 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:22631039
;
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:NP444638.RAC8DGxTQA6ODrBsa1MUDkKrtR7QycGotL9cSGgHY8X9Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}