@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0
> .
@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:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_head
{
this:
np:hasAssertion
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_assertion
;
np:hasProvenance
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_assertion
a
np:Assertion
.
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_provenance
a
np:Provenance
.
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_assertion
{
miriam-gene:1056
a
ncit:C16612
.
lld:C0342276
a
ncit:C7057
.
dgn-gda:DGN7903255c17004565d97f5974a37ee7fa
sio:SIO_000628
miriam-gene:1056
,
lld:C0342276
;
a
sio:SIO_001121
.
}
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_provenance
{
dgn-np:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_assertion
dcterms:description
"[Screening of 241 probands from suspected maturity-onset diabetes of the young (MODY) families negative for mutations in known MODY genes (95 individuals from Denmark and 146 individuals from UK) revealed no deletions in the proximal repeats of the CEL VNTR.]. 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:19760265
;
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:NP161985.RAIL5g-4X6tSffz1mCpvKQiAEhXpJM0Y53_VvnOiaWfr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}