@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU
> .
@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:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_head
{
this:
np:hasAssertion
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion
;
np:hasProvenance
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance
;
np:hasPublicationInfo
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion
a
np:Assertion
.
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance
a
np:Provenance
.
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion
{
miriam-gene:138804
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGNb25c5b9195a1cb19b22ef2ae7d264501
sio:SIO_000628
miriam-gene:138804
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance
{
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion
dcterms:description
"[When restricting the analysis to the subset of 38 patients who had molecular testing performed preoperatively on FNAB, the PPV and NPV of BRAF positivity for CLNM was 47 and 91%, respectively, and BRAF positivity was still a significant predictor of CLNM on both univariate (OR 8.4, p=0.01) and multivariate (OR 9.7, p=0.02) analyses.]. 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:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}