@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4
> .
@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:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_head
{
this:
np:hasAssertion
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_assertion
;
np:hasProvenance
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_assertion
a
np:Assertion
.
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_provenance
a
np:Provenance
.
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGN556fa31755ef194caee3057e6ad9ee09
sio:SIO_000628
miriam-gene:4297
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_provenance
{
dgn-np:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_assertion
dcterms:description
"[In this respect, data on ALL1 breakpoint localization suggest that similar pathogenetic mechanisms may underlie infant and TR AL and that these events might differ from those occurring in de novo AL.]. 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:9592986
;
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:NP238538.RAOP1tiHUh9TZsyy8zjckhtfzOdItopzCCj8woC1y1WZ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}