@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o
> .
@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:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_head
{
this:
np:hasAssertion
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion
;
np:hasProvenance
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion
a
np:Assertion
.
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance
a
np:Provenance
.
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0006413
a
ncit:C7057
.
dgn-gda:DGNca39b12aaf2138ca64204806066c9c82
sio:SIO_000628
miriam-gene:7157
,
lld:C0006413
;
a
sio:SIO_001121
.
}
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance
{
dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion
dcterms:description
"[Recent studies of the p53 gene in Burkitt's lymphomas have demonstrated that mutations are extremely common, and in fact it is rare that both alleles of the p53 gene in these tumors are not inactivated by mutation or deletion.]. 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:1437144
;
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:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}