@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ
> .
@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:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_head
{
this:
np:hasAssertion
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_assertion
;
np:hasProvenance
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_assertion
a
np:Assertion
.
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_provenance
a
np:Provenance
.
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_assertion
{
miriam-gene:6635
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN22152c8ba3abca4ff3754576d1f676fd
sio:SIO_000628
miriam-gene:6635
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_provenance
{
dgn-np:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_assertion
dcterms:description
"[B-RAF mutations, predominantly the specific V600E mutation and additional alterations in exons 11 and 15, were frequently detected in malignant melanomas, papillary thyroid tumors, and colorectal cancers with microsatellite instability (MSI).]. 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:16413100
;
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:NP685283.RAW40V81Te_qrsXwMIR2s946SQcZf-bKYke0SGLYvhHNQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}