@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4
> .
@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:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_head
{
this:
np:hasAssertion
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion
;
np:hasProvenance
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance
;
np:hasPublicationInfo
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion
a
np:Assertion
.
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance
a
np:Provenance
.
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion
{
miriam-gene:3159
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN831f42007d326380f43edfe386c51bb8
sio:SIO_000628
miriam-gene:3159
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance
{
dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion
dcterms:description
"[reported that the expression of the high mobility group (HMG) I(Y) proteins correlates with the malignant phenotype of human thyroid neoplasia, and suggested that the detection of the HMG I(Y) proteins might be a valid tool for an easy and sensitive discrimination assay between benign and malignant neoplastic thyroid disease.]. 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:10714095
;
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:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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
<
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> , <
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
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"v2.1.0" .
}