@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg
> .
@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:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_head
{
this:
np:hasAssertion
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion
;
np:hasProvenance
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance
;
np:hasPublicationInfo
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion
a
np:Assertion
.
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance
a
np:Provenance
.
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion
{
miriam-gene:54790
a
ncit:C16612
.
lld:C0026985
a
ncit:C7057
.
dgn-gda:DGN3dc9ab9b740651ac78b51c7f40cc79e6
sio:SIO_000628
miriam-gene:54790
,
lld:C0026985
;
a
sio:SIO_001121
.
}
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance
{
dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion
dcterms:description
"[A new study reports common mutations in the TET2 gene in myelodysplasia and related myeloid malignancies, suggesting that TET2 has an important role in hematopoiesis and in the pathogenesis of this disease.]. 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:19557078
;
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:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}