@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s
> .
@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:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_head
{
this:
np:hasAssertion
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_assertion
;
np:hasProvenance
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_assertion
a
np:Assertion
.
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_provenance
a
np:Provenance
.
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_assertion
{
miriam-gene:50484
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN5a42b24d94de7a3633458ce831f67be6
sio:SIO_000628
miriam-gene:50484
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_provenance
{
dgn-np:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_assertion
dcterms:description
"[Mutational analysis of p53R2 in 105 carcinomas including 15 cell lines also failed to detect any evidences for genomic deletion or somatic mutations leading to amino acid substitutions or frameshift whereas 31% (28 of 90) of the same primary tumors showed p53 alterations.]. 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:11920641
;
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:NP764082.RA1av7q2W7X8ja4yex8qckbkYJQUulHeaqmyoO5xFOw6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}