@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo
> .
@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:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_head
{
this:
np:hasAssertion
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_assertion
;
np:hasProvenance
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_assertion
a
np:Assertion
.
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_provenance
a
np:Provenance
.
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN9fb3537a72c9dfd627b49da9f76db181
sio:SIO_000628
miriam-gene:3630
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_provenance
{
dgn-np:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_assertion
dcterms:description
"[Because the INS gene, which was also translocated, is probably located proximal to HRAS1 on chromosome 11p, it is unlikely that HRAS1 was near the chromosome 11 breakpoint or involved in this leukaemia.]. 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:2713271
;
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:NP219832.RAybCngFAwzqwwqLg5xSTeODAGv7x-jgfG-0ygSTSyiEo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}