@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw
> .
@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:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_head
{
this:
np:hasAssertion
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_assertion
;
np:hasProvenance
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_assertion
a
np:Assertion
.
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_provenance
a
np:Provenance
.
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_assertion
{
miriam-gene:3145
a
ncit:C16612
.
lld:C1279945
a
ncit:C7057
.
dgn-gda:DGNe69973dec4d4078ec6f31a5561031810
sio:SIO_000628
miriam-gene:3145
,
lld:C1279945
;
a
sio:SIO_001121
.
}
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_provenance
{
dgn-np:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_assertion
dcterms:description
"[Our data showed large variations between the levels of mutant transcript in AIP patients and these variations did not correlate either to CRIM class, to the location of the disease causing mutation in the PBGD gene, or to the clinical phenotype of AIP.]. 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:9371741
;
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:NP467326.RA4FjC_1OZgqBaQDE2R820XM8uKI-07gtCfda9s86LJhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}