@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54
> .
@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:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_head
{
this:
np:hasAssertion
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_assertion
;
np:hasProvenance
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_provenance
;
np:hasPublicationInfo
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_assertion
a
np:Assertion
.
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_provenance
a
np:Provenance
.
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0751606
a
ncit:C7057
.
dgn-gda:DGNe2d6cd5ed16968e04b8ed81a183f7ade
sio:SIO_000628
miriam-gene:4436
,
lld:C0751606
;
a
sio:SIO_001121
.
}
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_provenance
{
dgn-np:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_assertion
dcterms:description
"[Leukemia cells with low levels of MSH2 contained partial or complete somatic deletions of one to four genes that regulate MSH2 degradation (FRAP1 (also known as MTOR), HERC1, PRKCZ and PIK3C2B); we also found these deletions in individuals with adult acute lymphoblastic leukemia (16%) and sporadic colorectal cancer (13.5%).]. 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:21946537
;
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:NP512762.RAK-kU7Bkixyq0ep3hHCNmyDx8Psqub0YyHNM8wGtku54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}