@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion
a
np:Assertion
.
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_provenance
a
np:Provenance
.
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN1cd225fa46aadb88567d71e9558f83e7
sio:SIO_000628
miriam-gene:3845
,
lld:C0023418
;
a
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.
}
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_provenance
{
dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion
dcterms:description
"[Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases.]. 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:23832011
;
prov:wasDerivedFrom
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;
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:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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