@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s
> .
@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:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_head
{
this:
np:hasAssertion
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_assertion
;
np:hasProvenance
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_assertion
a
np:Assertion
.
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_provenance
a
np:Provenance
.
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN32ea98df4cd6fdf553f1b14f68ab3b67
sio:SIO_000628
miriam-gene:3717
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_provenance
{
dgn-np:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_assertion
dcterms:description
"[Functional studies revealed subtle differences between the alternative forms, with the acute lymphoblastic leukemia variant showing higher activity, but reduced downstream signal transducer and activator of transcription activation and decreased sensitivity to JAK2 inhibition.]. 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:22733019
;
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:NP506568.RAGq2ikppD1mUA2Mfr5saG3joK75ySmwO95SeCkQ5bp0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}