@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs
> .
@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:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_head
{
this:
np:hasAssertion
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_assertion
;
np:hasProvenance
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_assertion
a
np:Assertion
.
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_provenance
a
np:Provenance
.
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_assertion
{
miriam-gene:796
a
ncit:C16612
.
lld:C0521158
a
ncit:C7057
.
dgn-gda:DGN92d48cfece5c0c08fcd7820dc0ee579a
sio:SIO_000628
miriam-gene:796
,
lld:C0521158
;
a
sio:SIO_001121
.
}
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_provenance
{
dgn-np:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_assertion
dcterms:description
"[It is concluded that 131I therapy as an adjunct to surgery is not indicated in the management of patients with residual hereditary MCT, although 131I may be of value in the prevention of tumor recurrence in patients with normal postoperative calcitonin values.]. 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:6746863
;
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:NP476503.RAjkgCqBH7hYG3ybZrM9pXkA3o7gPqgkC9egt7e1szPIs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}