@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs
> .
@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:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_head
{
this:
np:hasAssertion
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion
;
np:hasProvenance
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance
;
np:hasPublicationInfo
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion
a
np:Assertion
.
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance
a
np:Provenance
.
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN97dd2fbeff2526fa3491e88b1fa2e644
sio:SIO_000628
miriam-gene:7157
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_provenance
{
dgn-np:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_assertion
dcterms:description
"[p53 gene mutations are rarely detected at diagnosis in common haematological cancers such as multiple myeloma (MM), acute myeloid leukaemia (AML), chronic lymphocytic leukaemia (CLL) and Hodgkin's disease (HD), although their prevalence may increase with progression to more aggressive or advanced stages.]. 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:19955555
;
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:NP164589.RAuML_uv-NACr5uTiawJ5fIbImSVlbfbn3j_e2_AnHfxs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}