@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_head
{
this:
np:hasAssertion
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_assertion
;
np:hasProvenance
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_provenance
;
np:hasPublicationInfo
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_assertion
a
np:Assertion
.
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_provenance
a
np:Provenance
.
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0023480
a
ncit:C7057
.
dgn-gda:DGN1aa57a98ecd093f7b0b70c89a038828f
sio:SIO_000628
miriam-gene:3265
,
lld:C0023480
;
a
sio:SIO_001121
.
}
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_provenance
{
dgn-np:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_assertion
dcterms:description
"[To search for additional, novel RAS mutations, we sequenced all coding exons in NRAS, KRAS, and HRAS in 329 acute myeloid leukemia (AML) patients, 32 chronic myelomonocytic leukemia (CMML) patients, and 96 healthy individuals.]. 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:19075190
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP708791.RAA2t4Hex-mRNWj1TPdYA3J0dAHRJzvfjtP9MVU6sZWtE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:06+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}