@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs
> .
@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:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_head
{
this:
np:hasAssertion
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion
;
np:hasProvenance
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance
;
np:hasPublicationInfo
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion
a
np:Assertion
.
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance
a
np:Provenance
.
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNcdf3e5ede1e25a64a2e73c7c084b398c
sio:SIO_000628
miriam-gene:7157
,
lld:C0027651
;
a
sio:SIO_001122
.
}
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance
{
dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion
dcterms:description
"[We summarize here current knowledge on the respective roles of p53 mutagenesis and biological selection of mutations with specific functional characteristic in shaping the patterns and phenotypes of mutations observed in human cancers.]. 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:17401424
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:57+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" .
}