@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY
> .
@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:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_head
{
this:
np:hasAssertion
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_assertion
;
np:hasProvenance
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_assertion
a
np:Assertion
.
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_provenance
a
np:Provenance
.
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_assertion
{
miriam-gene:3557
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN39d8f6671dd9da42a23e97e9aa7cee24
sio:SIO_000628
miriam-gene:3557
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_provenance
{
dgn-np:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_assertion
dcterms:description
"[While in patients with chronic lymphocytic leukemia (CLL), hairy cell leukemia (HCL), multiple myeloma (MM) and related disorders, primary acute myeloid leukemia (AML), chronic myeloid leukemia (CML), and Hodgkin's disease (HD), the allelic distribution of IL-1RN was comparable to that seen in healthy control subjects, in a small group of patients with secondary AML the frequency of the IL-1RN*4 allele appeared to be significantly increased.]. 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:9384710
;
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:NP819560.RADofN9Iv0jQjGt3leoMDsyx_ig4xZ6SyuxAlYQhkYhvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}