@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI
> .
@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:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_head
{
this:
np:hasAssertion
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_assertion
;
np:hasProvenance
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_assertion
a
np:Assertion
.
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_provenance
a
np:Provenance
.
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN6f9562ce7e66eb4e76ade48d712db707
sio:SIO_000628
miriam-gene:472
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_provenance
{
dgn-np:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_assertion
dcterms:description
"[To address the ATA guidelines regarding the sequencing of the entire coding region of RET, we selected 50 patients with sporadic MTC (sMTC) without mutations in the hot spot regions of RET for extended investigation of exons 1-7, 9, 12, 17, 18, and 19.]. 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:22648435
;
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:NP761540.RAzE0xEzHTKovvv3Y0yzpVnWSi1D4y3-Vicwuz0ix5AaI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}