@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk
> .
@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:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_head
{
this:
np:hasAssertion
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_assertion
;
np:hasProvenance
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_provenance
;
np:hasPublicationInfo
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_assertion
a
np:Assertion
.
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_provenance
a
np:Provenance
.
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C2826177
a
ncit:C7057
.
dgn-gda:DGN5f119d5e0937ae2c85b23ff372cfe6c5
sio:SIO_000628
miriam-gene:4869
,
lld:C2826177
;
a
sio:SIO_001121
.
}
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_provenance
{
dgn-np:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_assertion
dcterms:description
"[Diagnosis of AML with mutated NPM1 can be done using molecular techniques, immunohistochemistry (looking at cytoplasmic dislocation of nucleophosmin that is predictive of NPM1 mutations) and Western blotting with antibodies specifically directed against NPM1 mutants.]. 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:20306250
;
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:NP276292.RAG2bXm7T1Z5vTkhARn4zOpi7Wb0Upu4uMY5gCW19x9kk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}