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http://rdf.disgenet.org/nanopublications.trig#NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_head
{
this:
np:hasAssertion
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_assertion
;
np:hasProvenance
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_provenance
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np:hasPublicationInfo
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_assertion
a
np:Assertion
.
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_provenance
a
np:Provenance
.
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_publicationInfo
a
np:PublicationInfo
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}
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{
miriam-gene:5979
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN39cc9453d000c0f4d258a31ee9f4af9c
sio:SIO_000628
miriam-gene:5979
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_provenance
{
dgn-np:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_assertion
dcterms:description
"[Using a proteomic-multiplexed analysis of the phosphotyrosine signaling together with antibody-based validation techniques, we identified several candidate molecules for RET (rearranged during transfection) tyrosine kinase receptor carrying mutations responsible for the multiple endocrine neoplasia type 2A and 2B (MEN2A and MEN2B) syndromes in two human medullary thyroid carcinoma (MTC) cell lines, TT and MZ-CRC-1, which express the RET-MEN2A and RET-MEN2B oncoproteins, respectively.]. 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:18756447
;
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:NP467505.RAlgp1ORHl6uZY60IOnbOGgLA9IyghqY9iZIMxr5huWjs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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
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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
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}