@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE
> .
@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:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_head
{
this:
np:hasAssertion
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_assertion
;
np:hasProvenance
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_assertion
a
np:Assertion
.
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_provenance
a
np:Provenance
.
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C3160732
a
ncit:C7057
.
dgn-gda:DGN1d638b2c2f845c60e3f85519b65b73a0
sio:SIO_000628
miriam-gene:7248
,
lld:C3160732
;
a
sio:SIO_001121
.
}
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_provenance
{
dgn-np:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_assertion
dcterms:description
"[DNA losses were most prevalent at 13q (75 per cent) and 4q (50 per cent), suggesting that inactivation of tumour suppressor genes at chromosomes 13q and 4q may be linked to sarcomatoid growth of RCC.]. 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:9828836
;
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:NP884931.RAH6oT1EfHl_4q0yS3DWKyDNhwOd3Dw9NWll9_rcGdJWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}