@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs
> .
@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:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_head
{
this:
np:hasAssertion
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_assertion
;
np:hasProvenance
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_provenance
;
np:hasPublicationInfo
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_assertion
a
np:Assertion
.
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_provenance
a
np:Provenance
.
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_assertion
{
miriam-gene:898
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN66e539c8596a44a2205d344cb0222154
sio:SIO_000628
miriam-gene:898
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_provenance
{
dgn-np:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_assertion
dcterms:description
"[Among 23 uterine serous carcinomas that were subjected to SNP array analysis, seven tumors with FBXW7 mutations (four tumors with point mutations, three tumors with hemizygous deletions) did not have CCNE1 amplification, and 13 (57%) tumors had either a molecular genetic alteration in FBXW7 or CCNE1 amplification.]. 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:22923510
;
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:NP403990.RAZ4QaVyx3oRkZm7kRDmApYji7N-ytga3XG5rWIEBRUgs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}