@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng
> .
@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:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_head
{
this:
np:hasAssertion
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion
;
np:hasProvenance
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance
;
np:hasPublicationInfo
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion
a
np:Assertion
.
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance
a
np:Provenance
.
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN89c11952313bfe93d2d2159a3c717e67
sio:SIO_000628
miriam-gene:3265
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance
{
dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion
dcterms:description
"[Mutations at codon 12, 13, and 61 of the HRAS, KRAS, and NRAS genes were evaluated in 99 cases of pediatric acute myeloid leukemia (AML) using oligonucleotide hybridization to polymerase chain reacted derived products.]. 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:2278970
;
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:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}