@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM
> .
@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:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_head
{
this:
np:hasAssertion
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_assertion
;
np:hasProvenance
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_assertion
a
np:Assertion
.
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_provenance
a
np:Provenance
.
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGN569cfeec7e9b833d18ed58262c2f6987
sio:SIO_000628
miriam-gene:673
,
lld:C0302592
;
a
sio:SIO_001121
.
}
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_provenance
{
dgn-np:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_assertion
dcterms:description
"[On the contrary, no mutation was identified in BRAF exon 15 for either endometrial or cervical cancer samples at position V600, which represents the most frequently mutated site of BRAF in human cancer.]. 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:16256179
;
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:NP395164.RAVSsxUS3cjN9NQR8TQm6hbcUoE-RyvN_nTa2hVosmoAM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}