@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ
> .
@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:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_head
{
this:
np:hasAssertion
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_assertion
;
np:hasProvenance
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_assertion
a
np:Assertion
.
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_provenance
a
np:Provenance
.
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_assertion
{
miriam-gene:113235
a
ncit:C16612
.
lld:C0030312
a
ncit:C7057
.
dgn-gda:DGN23c0f6e993af2f61f843fcfc2df6f1e0
sio:SIO_000628
miriam-gene:113235
,
lld:C0030312
;
a
sio:SIO_001121
.
}
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_provenance
{
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_assertion
dcterms:description
"[The PCFT-deficient mouse serves as a model for the hereditary folate malabsorption syndrome and is the most accurate animal model of folate deficiency anemia described to date that closely captures the spectrum of pathology typical of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:21346251
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP29977.RAEKKolMhgSxQ6TE15agcGHyxuaUv5VEC3o9PpGMIOkrQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:12+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" .
}