@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k
> .
@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:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_head
{
this:
np:hasAssertion
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion
;
np:hasProvenance
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion
a
np:Assertion
.
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance
a
np:Provenance
.
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion
{
miriam-gene:7161
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN6107920f4a30d04ef531b7e130cb4899
sio:SIO_000628
miriam-gene:7161
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_provenance
{
dgn-np:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_assertion
dcterms:description
"[Since it has been proposed that especially neoplasias lacking p53 alterations might show a loss of heterozygosity at 1p35-1p36, we studied the frequency of p53 and p73 deletions in bone marrow mononuclear cells of 68 patients with MM, two patients with monoclonal gammopathy of undetermined significance and four patients with plasma cell 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:10602435
;
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:NP291456.RAUfL_yBq4RbJoWCH1KtVo2AM-VXTafl-gN6DtYb7db8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}