@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk
> .
@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:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_head
{
this:
np:hasAssertion
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_assertion
;
np:hasProvenance
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_assertion
a
np:Assertion
.
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_provenance
a
np:Provenance
.
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN21976eaca055a6542c32e7578e307c94
sio:SIO_000628
miriam-gene:270
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_provenance
{
dgn-np:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_assertion
dcterms:description
"[We have previously shown that expression changes of the mitotic arrest deficiency (MAD) gene family plays a role in renal cell cancer (RCC) characterized by numerical chromosomal changes, namely papillary and chromophobe carcinomas, but nothing is known about the expression of mitotic checkpoint genes in the clear cell histotype (ccRCC).]. 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:18791270
;
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:NP820131.RAIA943AxRGC0eZCiCmJYWj2-3Xsqt4NrgE3yHTyS_SMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}