@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4
> .
@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:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_head
{
this:
np:hasAssertion
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_assertion
;
np:hasProvenance
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_provenance
;
np:hasPublicationInfo
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_assertion
a
np:Assertion
.
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_provenance
a
np:Provenance
.
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGN4fbb5aa9bc881c49f0675963c5be1dbc
sio:SIO_000628
miriam-gene:4893
,
lld:C0263214
;
a
sio:SIO_001121
.
}
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_provenance
{
dgn-np:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_assertion
dcterms:description
"[We analyzed 2502 patients with acute myeloid leukemia at diagnosis for NRAS mutations around the hot spots at codons 12, 13, and 61 and correlated the results to cytomorphology, cytogenetics, other molecular markers, and prognostic relevance of these mutations.]. 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:16434492
;
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:NP427567.RAQO5RD4sWz3B0dMYH_wqZMya5uXOIycBuXxAtuLDOip4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}