@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s
> .
@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:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_head
{
this:
np:hasAssertion
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_assertion
;
np:hasProvenance
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_assertion
a
np:Assertion
.
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_provenance
a
np:Provenance
.
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_assertion
{
miriam-gene:6208
a
ncit:C16612
.
lld:C1260899
a
ncit:C7057
.
dgn-gda:DGN133cccb3038d65fa8e5bdfa4d94c5eed
sio:SIO_000628
miriam-gene:6208
,
lld:C1260899
;
a
sio:SIO_001121
.
}
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_provenance
{
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_assertion
dcterms:description
"[Patients with nonclassical DBA and other hypoproliferative anemias may have somatically acquired 5q deletions with RPS14 haploinsufficiency not identified by fluorescence in situ hybridization or cytogenetic testing, thus refining the spectrum of disorders with 5q- deletions.]. 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:23943650
;
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 .
}
dgn-np:NP1102351.RABZ31etpMA49CuDhauXb8q3PtivXSTXlLeuYyY-1fr3s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:05+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}