@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_head
{
this:
np:hasAssertion
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_assertion
;
np:hasProvenance
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_provenance
;
np:hasPublicationInfo
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_assertion
a
np:Assertion
.
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_provenance
a
np:Provenance
.
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN9ea052668f8e7a7cfe34e33269bc4163
sio:SIO_000628
miriam-gene:5979
,
lld:C0549473
;
a
sio:SIO_001122
.
}
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_provenance
{
dgn-np:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_assertion
dcterms:description
"[ (1) BRAF(V599E) mutation and RET/PTC rearrangements were unique to PTC. The high prevalence of BRAF(V599E) mutation indicates that it is an important molecular hallmark of PTC. (2) BRAF(V599E) mutation rate was high in classic type PTC and tall cell type]. 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:16181547
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP95922.RAgwAywXd-oN5d8m8m0PjYHzGrY0SeCrLkHwlS5KEame4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}