@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg
> .
@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:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_head
{
this:
np:hasAssertion
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_assertion
;
np:hasProvenance
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_assertion
a
np:Assertion
.
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_provenance
a
np:Provenance
.
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0242621
a
ncit:C7057
.
dgn-gda:DGN80be6f20514275e77c929ccc76e5498a
sio:SIO_000628
miriam-gene:7157
,
lld:C0242621
;
a
sio:SIO_001121
.
}
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_provenance
{
dgn-np:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_assertion
dcterms:description
"[Loss of TP53 was caused by an isochromosome with breakpoints between 17p10 and 17p11.2 in four patients, an unbalanced translocation involving 17p10 to 17p11.2 in nine patients, and an unbalanced translocation involving 17p11.2 to 17p12 in three patients.]. 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:16737921
;
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:NP432490.RA55Exf0rLwazYJnbr2ijqt1fQUpoAgv9rYYAnwOcxZwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}