@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4
> .
@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:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_head
{
this:
np:hasAssertion
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_assertion
;
np:hasProvenance
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_assertion
a
np:Assertion
.
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_provenance
a
np:Provenance
.
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_assertion
{
miriam-gene:113235
a
ncit:C16612
.
lld:C0151482
a
ncit:C7057
.
dgn-gda:DGN3b575dbb2a43cd2c751a495f003cddf6
sio:SIO_000628
miriam-gene:113235
,
lld:C0151482
;
a
sio:SIO_001121
.
}
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_provenance
{
dgn-np:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_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_literature
;
sio:SIO_000772
miriam-pubmed:21346251
;
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:NP938735.RABMJOuId37rTmYkAq07eYpvoFO5hYS6MVDqT1Km2LeM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}