@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM
> .
@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:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_head
{
this:
np:hasAssertion
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion
;
np:hasProvenance
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance
;
np:hasPublicationInfo
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion
a
np:Assertion
.
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance
a
np:Provenance
.
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion
{
miriam-gene:57498
a
ncit:C16612
.
lld:C0023484
a
ncit:C7057
.
dgn-gda:DGN9c01872137330bfb326e9b1aa4375079
sio:SIO_000628
miriam-gene:57498
,
lld:C0023484
;
a
sio:SIO_001121
.
}
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance
{
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion
dcterms:description
"[Using allele-specific amplification method (ARMS), a highly sensitive one-stage allele-specific PCR, we have evaluated the incidence of NRAS and KRAS2 activating mutations (codons 12, 13, and 61) in 62 patients with either monoclonal gammopathy of undetermined significance (MGUS) or multiple myeloma (MM), primary plasma-cell leukemia (P-PCL), and also in human myeloma cell lines (HMCL).]. 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:11524732
;
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:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}