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http://rdf.disgenet.org/nanopublications.trig#NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA
> .
@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#
> .
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{
this:
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_assertion
a
np:Assertion
.
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_provenance
a
np:Provenance
.
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGNd9725c191dc7d57c219ca42b7f3f2cac
sio:SIO_000628
miriam-gene:7157
,
lld:C1333600
;
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.
}
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_provenance
{
dgn-np:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_assertion
dcterms:description
"[In this report, we address the possibility that some sporadic sarcomas may be associated with new germline mutations of the p53 gene, which would not be manifested as familial cancer unless the patient survived to reproduce.]. 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:1565143
;
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:NP364829.RAEhfAHAwNH-LSgOV23RkXn17hF7tjSscL_LloM5XkStA130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
<
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> , <
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> , <
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> ;
pav:createdBy
<
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