@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs
> .
@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:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_head
{
this:
np:hasAssertion
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_assertion
;
np:hasProvenance
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_provenance
;
np:hasPublicationInfo
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_assertion
a
np:Assertion
.
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_provenance
a
np:Provenance
.
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0007133
a
ncit:C7057
.
dgn-gda:DGN19daa7c51d63e7e887adf11619bfa1ea
sio:SIO_000628
miriam-gene:5979
,
lld:C0007133
;
a
sio:SIO_001121
.
}
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_provenance
{
dgn-np:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_assertion
dcterms:description
"[The two rearrangements resulting from inversion of part of chromosome 10 (PTC1 and PTC3) accounted for the majority of RET rearrangements identified, with PTC1 being associated with papillary carcinomas of the classic and diffuse sclerosing variants and PTC3 with the solid/follicular variant.]. 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:10646883
;
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:NP273252.RAO08m3oIb-NFd_lAjnYv2E0I1Wxj4WFSJQqQSyLKfFDs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:49+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}