@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion
;
np:hasProvenance
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance
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np:hasPublicationInfo
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion
a
np:Assertion
.
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance
a
np:Provenance
.
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7157
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN4adcfaf08d723e93e6af50a3091b0740
sio:SIO_000628
miriam-gene:7157
,
lld:C0018939
;
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.
}
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_provenance
{
dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_assertion
dcterms:description
"[In this review we will discuss: 5q- syndrome mouse models, the possible mechanisms underlying this blood disorder with respect to the candidate genes and comparisons with other ribosomopathies and the involvement of the p53 pathway in these diseases.]. 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:20980806
;
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 .
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dgn-np:NP901517.RAm8oCdK9OrH0RtsbfMpIRIPz1xeKCT-ZSM5QcV67zTQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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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> , <
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> , <
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" .
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"v2.1.0" .
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