@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4
> .
@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:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_head
{
this:
np:hasAssertion
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_assertion
;
np:hasProvenance
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_provenance
;
np:hasPublicationInfo
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_assertion
a
np:Assertion
.
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_provenance
a
np:Provenance
.
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0023443
a
ncit:C7057
.
dgn-gda:DGN2f393cab484b1272aaf9a712a7573739
sio:SIO_000628
miriam-gene:673
,
lld:C0023443
;
a
sio:SIO_001121
.
}
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_provenance
{
dgn-np:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_assertion
dcterms:description
"[The high prevalence of BRAF(V600E) activating mutation in papillary thyroid carcinoma, cutaneous malignant melanoma and hairy cell leukemia implies that the mutation is an important 'driver' or 'codriver' in the development of a subset of these cancers.]. 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:22369373
;
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:NP440657.RA2yyI6zMxkNFVNYxdEIWyUlsA1TB8uyUjbSYknW9ViC4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}