@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI
> .
@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:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_head
{
this:
np:hasAssertion
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_assertion
;
np:hasProvenance
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_assertion
a
np:Assertion
.
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_provenance
a
np:Provenance
.
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_assertion
{
miriam-gene:7066
a
ncit:C16612
.
lld:C0836924
a
ncit:C7057
.
dgn-gda:DGNa82269c88169df0844feb44e18d08496
sio:SIO_000628
miriam-gene:7066
,
lld:C0836924
;
a
sio:SIO_001121
.
}
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_provenance
{
dgn-np:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_assertion
dcterms:description
"[Mutations that restructure this mRNA in ways that elevate production of thrombopoietin cause hereditary thrombocythemia, demonstrating that some mRNAs are designed deliberately with upstream AUG codons to preclude efficient translation and thus to prevent harmful overproduction of potent proteins.]. 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:12226704
;
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:NP301533.RAWnpWUhagD-vfQaOhSWfkOwbCLgrsyb78gg47J0oIFtI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}