@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc
> .
@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:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_head
{
this:
np:hasAssertion
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_assertion
;
np:hasProvenance
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_provenance
;
np:hasPublicationInfo
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_assertion
a
np:Assertion
.
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_provenance
a
np:Provenance
.
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNcc8154d99cbe7715214f8ee7d4b147be
sio:SIO_000628
miriam-gene:1630
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_provenance
{
dgn-np:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_assertion
dcterms:description
"[Deletion of the p53 gene on chromosome 17p, deletion of the DCC gene on 18q, and high fractional allelic loss (fraction of evaluable nonacrocentric autosomal arms with deletion) have been associated with distant metastases and with poorer prognosis in patients without initial evidence of disseminated disease.]. 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:1540900
;
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:NP501081.RAktVqfsVOz-B4hGNnBSQ6g5h5LkhNAtjExXZVxZ3LqWc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}