@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo
> .
@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:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_head
{
this:
np:hasAssertion
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_assertion
;
np:hasProvenance
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_provenance
;
np:hasPublicationInfo
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_assertion
a
np:Assertion
.
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_provenance
a
np:Provenance
.
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0023480
a
ncit:C7057
.
dgn-gda:DGNde239fa3b041d6325ff30d8ca075cf12
sio:SIO_000628
miriam-gene:4893
,
lld:C0023480
;
a
sio:SIO_001121
.
}
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_provenance
{
dgn-np:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_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-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:NP725172.RA68O4NtkJRtLpk0-eGUvaQQmoGmsKQLVkqRBzGGiy9qo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}