@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg
> .
@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:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_head
{
this:
np:hasAssertion
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_assertion
;
np:hasProvenance
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_provenance
;
np:hasPublicationInfo
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_assertion
a
np:Assertion
.
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_provenance
a
np:Provenance
.
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_assertion
{
miriam-gene:2548
a
ncit:C16612
.
lld:C0162872
a
ncit:C7057
.
dgn-gda:DGN1477650dd4b887d040fbbc59eadd41de
sio:SIO_000628
miriam-gene:2548
,
lld:C0162872
;
a
sio:SIO_001121
.
}
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_provenance
{
dgn-np:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_assertion
dcterms:description
"[A nonsense mutation was identified at codon 526 (GAA to TAA, glutamine to termination) in two cell lines (UMSCC22A and UMSCC22B) derived from the primary tumor and lymph node metastasis of the same patient.]. 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:8653689
;
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:NP588651.RAS-1nlmeGtrl8yBrl95Z8MLw508GumF58elBxJjEt6zg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}