@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY
> .
@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:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_head
{
this:
np:hasAssertion
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_assertion
;
np:hasProvenance
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_provenance
;
np:hasPublicationInfo
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_assertion
a
np:Assertion
.
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_provenance
a
np:Provenance
.
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_assertion
{
miriam-gene:4597
a
ncit:C16612
.
lld:C0221013
a
ncit:C7057
.
dgn-gda:DGN45cd93a6e832d051f35009e8fd6bb70c
sio:SIO_000628
miriam-gene:4597
,
lld:C0221013
;
a
sio:SIO_001121
.
}
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_provenance
{
dgn-np:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_assertion
dcterms:description
"[Control experiments showed that 10 indolent SM patients without associated MPD did not carry the JAK2 mutation V617F and that 15 CIMF patients without SM did not carry the KIT mutation D816V.]. 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:18165278
;
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:NP820370.RAmTjNAdjtownpeVh_zxV961QR7gLDPInG_J8B78hYZYY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}