@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI
> .
@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:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_head
{
this:
np:hasAssertion
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_assertion
;
np:hasProvenance
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_assertion
a
np:Assertion
.
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_provenance
a
np:Provenance
.
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_assertion
{
miriam-gene:28956
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN0b1ef88fdf3d9cd31498e1498488f9cb
sio:SIO_000628
miriam-gene:28956
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_provenance
{
dgn-np:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_assertion
dcterms:description
"[Testing by qPCR of 18 bone marrow specimens from paediatric acute lymphoblastic leukaemia (ALL) patients at diagnosis revealed nine to be GG, six to be GD and three to be DD for exon 2 of p14(ARF)/p16(INK4A), concordant with Southern blotting analysis.]. 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:15607365
;
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:NP734123.RA_ILhaEo0cmUuViHkkw8xIW9L1CyNYNjnRLsmfvoiHJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}