@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w
> .
@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:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_head
{
this:
np:hasAssertion
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_assertion
;
np:hasProvenance
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_provenance
;
np:hasPublicationInfo
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_assertion
a
np:Assertion
.
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_provenance
a
np:Provenance
.
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_assertion
{
miriam-gene:6208
a
ncit:C16612
.
lld:C1292779
a
ncit:C7057
.
dgn-gda:DGN7680ba9b19a1b5924a96f671a550a98b
sio:SIO_000628
miriam-gene:6208
,
lld:C1292779
;
a
sio:SIO_001121
.
}
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_provenance
{
dgn-np:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_assertion
dcterms:description
"[The commonly deleted region in 5q- syndrome, which is distinct from that in patients with complex cytogenetic changes that include del(5q), includes the ribosomal protein S14 locus and it has been proposed that that loss of an RPS14 allele accounts for the 5q- syndrome phenotype.]. 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:19016715
;
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:NP284886.RALgESilP1gBum78tVNxRcjO5AK6iJnBE9iozoTsWLv0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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
;
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" .
}