@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU
> .
@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:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_head
{
this:
np:hasAssertion
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_assertion
;
np:hasProvenance
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_provenance
;
np:hasPublicationInfo
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_assertion
a
np:Assertion
.
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_provenance
a
np:Provenance
.
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1861305
a
ncit:C7057
.
dgn-gda:DGNd33a3a3937cfdc7066dbc37bda6b1c09
sio:SIO_000628
miriam-gene:7248
,
lld:C1861305
;
a
sio:SIO_001121
.
}
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_provenance
{
dgn-np:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_assertion
dcterms:description
"[While the high frequency of chromosome 9q loss in TCC may reflect destabilization of the chromosome related to hypomethylation of repetitive DNA, the data are compatible with the existence of tumour suppressor genes on this chromosome arm.]. 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:11747331
;
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:NP700159.RAeGzovQLJ7pc_Hu-hAucqo2KDIK9nEMBNL6W3IsizTiU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}