@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_head
{
this:
np:hasAssertion
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_assertion
;
np:hasProvenance
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_provenance
;
np:hasPublicationInfo
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_assertion
a
np:Assertion
.
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_provenance
a
np:Provenance
.
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN2e54247c273758548f50607cd83580ba
sio:SIO_000628
miriam-gene:2623
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_provenance
{
dgn-np:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_assertion
dcterms:description
"[Furthermore, few would have guessed that missense mutations in GATA1 would cause inherited blood disorders, while acquired mutations would be found associated with essentially all cases of acute megakaryoblastic leukemia (AMKL) in children with Down syndrome (DS).]. 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:15659348
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP476918.RAH9mFAsWylQDzyUo4AlgB01y_nGSddZ0jGvXzmNj8VoU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}