@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4
> .
@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:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_head
{
this:
np:hasAssertion
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_assertion
;
np:hasProvenance
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_assertion
a
np:Assertion
.
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_provenance
a
np:Provenance
.
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGN5ad22268b16f9d2b5845662d44695040
sio:SIO_000628
miriam-gene:673
,
lld:C0007115
;
a
sio:SIO_001122
.
}
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_provenance
{
dgn-np:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_assertion
dcterms:description
"[BRAF(T1799A) mutation is the most prevalent genetic alteration in thyroid cancers and is specific for PTC, characteristics that make it the most potentially helpful genetic tool to improve the diagnostic accuracy of FNAB.]. 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:22504197
;
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:NP974903.RAqlRrSsvoP6tI_XURPi4EdUEl2dCMNomIT5yQpiUutI4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:06+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" .
}