@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k
> .
@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:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_head
{
this:
np:hasAssertion
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_assertion
;
np:hasProvenance
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_assertion
a
np:Assertion
.
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_provenance
a
np:Provenance
.
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0004698
a
ncit:C7057
.
dgn-gda:DGNd2062064df0ae7ee67e8452a8c5c9333
sio:SIO_000628
miriam-gene:7157
,
lld:C0004698
;
a
sio:SIO_001122
.
}
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_provenance
{
dgn-np:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_assertion
dcterms:description
"[In this study, based on the hypothesis that the genetic pathways leading to BEN might be associated with p53 dysfunction, we screened for p53 gene mutations 90 Bulgarian BEN patients using optimized PCR-SSCP-sequencing analysis.]. 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:16487937
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92859.RA7PQJe649EMAigZuuCJDkCGUx6xs4u0v79G0lQnSom6k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
}