@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0
> .
@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:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_head
{
this:
np:hasAssertion
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_assertion
;
np:hasProvenance
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_assertion
a
np:Assertion
.
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_provenance
a
np:Provenance
.
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0280856
a
ncit:C7057
.
dgn-gda:DGN600fa8a6b50328b2ed5607521fcca227
sio:SIO_000628
miriam-gene:7157
,
lld:C0280856
;
a
sio:SIO_001121
.
}
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_provenance
{
dgn-np:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_assertion
dcterms:description
"[We have sought to determine the basis for preferential loss of the codon 72 proline (72P) rather than the arginine (72R) allele in squamous cell carcinoma of the vulva with loss of heterozygosity (LOH) in p53.]. 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:11156383
;
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:NP349370.RAVaJEmYgN_gqLcBbpQpsd3UalAwH8rO5MLtTiKhBBuM0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}