@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI
> .
@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:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_head
{
this:
np:hasAssertion
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_assertion
;
np:hasProvenance
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_provenance
;
np:hasPublicationInfo
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_assertion
a
np:Assertion
.
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_provenance
a
np:Provenance
.
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_assertion
{
miriam-gene:7126
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN1c4585c7185b6f344ba614800cb4575c
sio:SIO_000628
miriam-gene:7126
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_provenance
{
dgn-np:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_assertion
dcterms:description
"[Since the dU suppression test is abnormal in transcobalamin II deficiency and in some congenital disorders of vitamin B12 and folate metabolism, it is very useful in the investigation of obscure anaemias in infancy and childhood.]. 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:NP774341.RAr7LvGxn2VlpnCahHL8FnY2t9Sp-WIcu_zgCjcvy7FPI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}