@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE
> .
@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:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_head
{
this:
np:hasAssertion
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion
;
np:hasProvenance
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance
;
np:hasPublicationInfo
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion
a
np:Assertion
.
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance
a
np:Provenance
.
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion
{
miriam-gene:1436
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN5cabb1543cf8aa774f1f08b399fbfb5b
sio:SIO_000628
miriam-gene:1436
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance
{
dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion
dcterms:description
"[Cases in point are the detection of RAS and FMS mutations in healthy individuals who had been treated in the past with cytotoxic therapy for lymphoma, the frequent observation of clonal remission in AML patients, or the identification of oncogene mutations in healthy individuals without even a history of malignancy or chemotherapy.]. 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:1613006
;
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:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:06+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" .
}