@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs
> .
@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:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_head
{
this:
np:hasAssertion
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_assertion
;
np:hasProvenance
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_provenance
;
np:hasPublicationInfo
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_assertion
a
np:Assertion
.
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_provenance
a
np:Provenance
.
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN93b8fdbae0b4d9ff837516efae351028
sio:SIO_000628
miriam-gene:472
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_provenance
{
dgn-np:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_assertion
dcterms:description
"[ATA guidelines that includes risk assessment of RET mutation are important in predicting the presence of MTC in patients who are candidates for prophylactic thyroidectomy and in determining the timing of operative resection.]. 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:21134565
;
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:NP830809.RAk5Q3mE8JLXjOaSOrLmX2zfK_3GbvSwyMKNER6rdsxVs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}