@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A
> .
@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:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_head
{
this:
np:hasAssertion
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_assertion
;
np:hasProvenance
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_assertion
a
np:Assertion
.
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_provenance
a
np:Provenance
.
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0751606
a
ncit:C7057
.
dgn-gda:DGN170f49704d0efe7137409b10ad9ce102
sio:SIO_000628
miriam-gene:1030
,
lld:C0751606
;
a
sio:SIO_001121
.
}
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_provenance
{
dgn-np:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_assertion
dcterms:description
"[Hypermethylation of p15INK4B, without alteration of p16INK4A, was an almost universal finding in adult acute myelogenous leukemia, and occurred very frequently in adult acute lymphocytic leukemia and pediatric acute myelogenous leukemia and acute lymphocytic leukemia.]. 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:9041182
;
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:NP578903.RALEX1dw81jZ_boVRu742UdGWJhJ0LJyRO8Mx1OuRii-A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}