@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_assertion
;
np:hasProvenance
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_provenance
;
np:hasPublicationInfo
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_assertion
a
np:Assertion
.
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_provenance
a
np:Provenance
.
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:6777
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGNd348965d0ef6737bffd96cb8e5fe8189
sio:SIO_000628
miriam-gene:6777
,
lld:C0040028
;
a
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.
}
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_provenance
{
dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_assertion
dcterms:description
"[To evaluate the frequency of MPL W515L, W515K and S505N mutations in essential thrombocythemia (ET) and primary myelofibrosis (PMF) and to determine whether MPLW515L leads to impaired Mpl expression, constitutive STAT3 and STAT5 activation and enhanced response to thrombopoietin (TPO).]. 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:20113333
;
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 .
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dgn-np:NP764019.RAcGBKEy-4gqcT78uMc4a8DSy071-JNvmt8gniFuDe7fo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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
<
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> , <
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
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