@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE
> .
@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:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_head
{
this:
np:hasAssertion
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_assertion
;
np:hasProvenance
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_provenance
;
np:hasPublicationInfo
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_assertion
a
np:Assertion
.
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_provenance
a
np:Provenance
.
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGN3d65ec1a60858d78c3b0fe383fca0c94
sio:SIO_000628
miriam-gene:673
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_provenance
{
dgn-np:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_assertion
dcterms:description
"[Of the commonly used clinical parameters available preoperatively, the BRAF V600E mutation is the only independent predictor of CLNM in PTC and can be utilized to guide the extent of initial surgery.]. 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:22941165
;
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:NP170800.RAUbh5idIHN9TOwW5Izjrd0XgPG8GNJ6u8jpNxufOZ7KE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}