@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw
> .
@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:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_head
{
this:
np:hasAssertion
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_assertion
;
np:hasProvenance
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_provenance
;
np:hasPublicationInfo
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_assertion
a
np:Assertion
.
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_provenance
a
np:Provenance
.
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_assertion
{
miriam-gene:3558
a
ncit:C16612
.
lld:C0206141
a
ncit:C7057
.
dgn-gda:DGN1328f53328b90cc5bb7dd0c94396f98b
sio:SIO_000628
miriam-gene:3558
,
lld:C0206141
;
a
sio:SIO_001121
.
}
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_provenance
{
dgn-np:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_assertion
dcterms:description
"[Hypodense activated eosinophils have been described in various diseases such as parasitic or allergic diseases, hypereosinophilic syndrome (HES) associated in some cases to myeloproliferative markers, and more recently described in patients undergoing recombinant IL2 treatment.]. 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:2037012
;
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:NP648090.RAaescmA-QVRpUiclIy73lQCsQCX_E7X7MsOJorEKF_Qw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}