@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ
> .
@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:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_head
{
this:
np:hasAssertion
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_assertion
;
np:hasProvenance
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_assertion
a
np:Assertion
.
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_provenance
a
np:Provenance
.
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGNe634fa17083c527f4f98672f69134120
sio:SIO_000628
miriam-gene:5781
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_provenance
{
dgn-np:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_assertion
dcterms:description
"[To test the hypothesis that PTPN11 mutations might contribute to myeloid leukemogenesis, we screened the entire coding region for mutations in 51 JMML specimens and in selected exons from 60 patients with other myeloid malignancies.]. 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:14644997
;
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:NP558095.RAx53FP_Lr7Z08ioSYt0bF_-fxxAutZ4xPTjrqFr10CRQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}