@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs
> .
@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:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_head
{
this:
np:hasAssertion
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_assertion
;
np:hasProvenance
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_assertion
a
np:Assertion
.
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_provenance
a
np:Provenance
.
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_assertion
{
miriam-gene:7954
a
ncit:C16612
.
lld:C0271979
a
ncit:C7057
.
dgn-gda:DGNc9129a2324f7bdc2f3f940452110e74d
sio:SIO_000628
miriam-gene:7954
,
lld:C0271979
;
a
sio:SIO_001121
.
}
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_provenance
{
dgn-np:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_assertion
dcterms:description
"[Further studies of subjects with high HbF and benign conditions, such as HPFH, could be of help in clarifying this point, to the aim of safely increasing HbF in thalassemia intermedia.]. 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:8952151
;
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:NP393029.RAROig5RWgbgVbr365AaUXdsN0psJ1SvVRuZt_vdYKyvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}