@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg
> .
@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:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_head
{
this:
np:hasAssertion
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_assertion
;
np:hasProvenance
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_provenance
;
np:hasPublicationInfo
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_assertion
a
np:Assertion
.
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_provenance
a
np:Provenance
.
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_assertion
{
miriam-gene:8031
a
ncit:C16612
.
lld:C0007133
a
ncit:C7057
.
dgn-gda:DGN25fa53223c39063f47fc74094b867c4c
sio:SIO_000628
miriam-gene:8031
,
lld:C0007133
;
a
sio:SIO_001121
.
}
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_provenance
{
dgn-np:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_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-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:NP628935.RACTh2ls6Qi6LZRdk-h2YIttv_6Qw3R5E1nmxVT4wS9vg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}