@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI
> .
@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:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_head
{
this:
np:hasAssertion
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_assertion
;
np:hasProvenance
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_assertion
a
np:Assertion
.
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_provenance
a
np:Provenance
.
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_assertion
{
miriam-gene:10771
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGN6cb5c7b4ab91ba26369256ae676b0760
sio:SIO_000628
miriam-gene:10771
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_provenance
{
dgn-np:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_assertion
dcterms:description
"[We found significant association between the CNVs of BS69 and these hematological malignancies including acute lymphoblastic leukemia (ALL), acute myelogenous leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), multiple myeloma (MM), and myelodysplastic syndrome (MDS).]. 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:20425112
;
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:NP517222.RAkpMFUQg5fObxirjFIdsNTWqTu7GxkW8QI8hrYGQmmNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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" .
}