@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk
> .
@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:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_head
{
this:
np:hasAssertion
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_assertion
;
np:hasProvenance
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_provenance
;
np:hasPublicationInfo
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_assertion
a
np:Assertion
.
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_provenance
a
np:Provenance
.
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGNc706773552f6d8252dc8de3a836c7bb2
sio:SIO_000628
miriam-gene:3643
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_provenance
{
dgn-np:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_assertion
dcterms:description
"[Humans with congenital absence of the islets of Langerhans and mice rendered null for the insulin receptor rapidly develop severe hyperglycemia and ketoacidosis and, if untreated, die in the early neonatal period.]. 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:11443207
;
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:NP931224.RAGZhe1vhOGc6ufL4F_duFG0uesB972pdlgPmKRdLVeLk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}