@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc
> .
@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:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_head
{
this:
np:hasAssertion
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_assertion
;
np:hasProvenance
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_provenance
;
np:hasPublicationInfo
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_assertion
a
np:Assertion
.
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_provenance
a
np:Provenance
.
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0023462
a
ncit:C7057
.
dgn-gda:DGN64380f088d6bff5c89a78c0c3f4865b7
sio:SIO_000628
miriam-gene:2623
,
lld:C0023462
;
a
sio:SIO_001121
.
}
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_provenance
{
dgn-np:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_assertion
dcterms:description
"[Four years ago it was discovered that nearly all cases of transient myeloproliferative disorder and acute megakaryocytic leukemia in children with Down syndrome acquire mutations in the hematopoietic transcription factor gene GATA1.]. 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:17224656
;
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:NP190110.RAsGydOQU9QV2Fs6KsFwCcDvVhCfgKemcVx2u6FIYSnbc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}