@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_assertion
a
np:Assertion
.
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
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{
miriam-gene:55733
a
ncit:C16612
.
lld:C0270814
a
ncit:C7057
.
dgn-gda:DGN8960e2ddbfff8dd438df7dee45f7bf2d
sio:SIO_000628
miriam-gene:55733
,
lld:C0270814
;
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.
}
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_provenance
{
dgn-np:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_assertion
dcterms:description
"[Adding our new findings to the existing data clearly reveals a mutational hotspot, with 73% (24 out of 33) of the hitherto described unrelated patients having mutations in a stretch of five SKI residues (from p.(Ser31) to p.(Pro35)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24736733
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1173837.RAmbQCkzhcjlZcbfklFBYBscRgXyRAPgZF_RwOMLZ9bk4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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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
> ;
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<
http://orcid.org/0000-0003-0169-8159
> ;
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"v4.0.0.0" .
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"v4.0.0" .
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