@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E
> .
@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:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_head
{
this:
np:hasAssertion
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_assertion
;
np:hasProvenance
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_provenance
;
np:hasPublicationInfo
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_assertion
a
np:Assertion
.
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_provenance
a
np:Provenance
.
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGN81e63f6ff01641e939dc08fade63052c
sio:SIO_000628
miriam-gene:7157
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_provenance
{
dgn-np:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_assertion
dcterms:description
"[These data suggested that disruptions of both genes are extremely rare in MPD in chronic phase and that loss of functions in the p53 gene could be involved in progression of MPD such as PV and ET.]. 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:12353315
;
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:NP769519.RAcfooJkyuVvVzeI2i_J2mB-lk2r5f8CHQ4tK7qEKJj-E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}