@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4
> .
@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:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_head
{
this:
np:hasAssertion
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_assertion
;
np:hasProvenance
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_assertion
a
np:Assertion
.
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_provenance
a
np:Provenance
.
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1368683
a
ncit:C7057
.
dgn-gda:DGN94801b13613398579543e68bca7415e3
sio:SIO_000628
miriam-gene:7157
,
lld:C1368683
;
a
sio:SIO_001121
.
}
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_provenance
{
dgn-np:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_assertion
dcterms:description
"[Since point mutations in the p53 gene appear to be important in the process of transformation in many epithelial tumors, we looked for these mutations in the critical regions of the p53 gene (exons 4, 5, 6, 7, and 8).]. 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:8464238
;
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:NP484853.RAI8bu9ZE-dYr_aotjaObRahEM-vF4QpzXfvaRn8TixS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}