@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM
> .
@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/v3.0.0/void/
> .
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_head
{
this:
np:hasAssertion
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_assertion
;
np:hasProvenance
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_provenance
;
np:hasPublicationInfo
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_assertion
a
np:Assertion
.
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_provenance
a
np:Provenance
.
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_assertion
{
miriam-gene:8890
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNb94ba35f53dd8331142c66fc7c0bca70
sio:SIO_000628
miriam-gene:8890
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_provenance
{
dgn-np:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_assertion
dcterms:description
"[The large clinical spectrum observed from the more severe antenatal forms responsible for fetal death to milder adult forms with an onset after 16 years old and restricted to slow cognitive impairment have lead to the concept of eIF2B-related disorders.]. 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:20016818
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP810399.RAObKgwpFhxz_A8yaSTebfVXTj0vtmNrnj9CL4H2bfwvM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:51+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}