@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI
> .
@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:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_head
{
this:
np:hasAssertion
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_assertion
;
np:hasProvenance
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_assertion
a
np:Assertion
.
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_provenance
a
np:Provenance
.
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_assertion
{
miriam-gene:7126
a
ncit:C16612
.
lld:C0085662
a
ncit:C7057
.
dgn-gda:DGNcf4a6aa3e84fd96f34ab66d48bae796e
sio:SIO_000628
miriam-gene:7126
,
lld:C0085662
;
a
sio:SIO_001121
.
}
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_provenance
{
dgn-np:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_assertion
dcterms:description
"[For these reasons, the dU suppression test has been adopted by several laboratories across the world for investigating patients with (a) possible vitamin B12 or folate deficiency, (b) macrocytosis, and (c) megaloblastic erythropoiesis.]. 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:3052662
;
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:NP412247.RA1_gN8W_v7Sq7ixXPMdhZVEAho2bf2S9smnk-hjsZAMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}