@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE
> .
@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:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_head
{
this:
np:hasAssertion
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion
;
np:hasProvenance
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion
a
np:Assertion
.
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance
a
np:Provenance
.
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGN7c5e37c09c65fe734b8c9abb733fce50
sio:SIO_000628
miriam-gene:673
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_provenance
{
dgn-np:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_assertion
dcterms:description
"[Current selection of PTC patients for CND is appropriate but higher extent of the procedure, once selected, is needed to reduce disease recurrence, which may be defined by combination use of preoperative BRAF mutation testing and conventional risk factors of PTC.]. 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:23132792
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1026530.RAtPNdyZ6hERwJq0sXMGeQGo2dbxot8qHbbbkbkBgOQeE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:31+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" .
}