@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs
> .
@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:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_head
{
this:
np:hasAssertion
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_assertion
;
np:hasProvenance
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_assertion
a
np:Assertion
.
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_provenance
a
np:Provenance
.
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGNa77e1e72dd39bc04a2b4114aa357383a
sio:SIO_000628
miriam-gene:673
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_provenance
{
dgn-np:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_assertion
dcterms:description
"[Highly sensitive and specific molecular assays such as MEMO sequencing are optimal for detecting the BRAF mutations in thyroid FNAC because these techniques can detect PTC that might be missed by cytology or less sensitive molecular assays.]. 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:22500044
;
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:NP974622.RA_OHgxDoxh2yCVUN0-daioAgHV4yn5Ky8rMnDIeoaoQs130_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
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;
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" .
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pav:version
"v4.0.0" .
}