@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA
> .
@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:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_head
{
this:
np:hasAssertion
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_assertion
;
np:hasProvenance
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_provenance
;
np:hasPublicationInfo
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_assertion
a
np:Assertion
.
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_provenance
a
np:Provenance
.
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGNcb437eee6d43e7360c0b4e8e1d4e11e5
sio:SIO_000628
miriam-gene:3265
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_provenance
{
dgn-np:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_assertion
dcterms:description
"[A heterozygous deleted mutation was detected in K-RAS oncogene (exon 2) in agarose gel electrophoresis in one patient and point or substitution mutations are detected using single strand conformational polymorphism (SSCP) in other different patients with bladder cancer (4/14).]. 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:12092657
;
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:NP253459.RAOW7vc6miaBn49IwhsRedsEhZVI6N3A-gsRdOej8QcdA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}