@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0
> .
@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:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_head
{
this:
np:hasAssertion
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_assertion
;
np:hasProvenance
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_assertion
a
np:Assertion
.
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_provenance
a
np:Provenance
.
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_assertion
{
miriam-gene:7126
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGNdf8d315b6e2d9a28785cc2a3a19c95b5
sio:SIO_000628
miriam-gene:7126
,
lld:C0598608
;
a
sio:SIO_001121
.
}
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_provenance
{
dgn-np:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_assertion
dcterms:description
"[Since vitamin B12 serves as a cofactor in the synthesis of methyl precursors for biological methylation and enables methylfolate to be recycled for nucleotide synthesis, B12 deficiency has been known to induce hyperhomocysteinemia and inadequate DNA synthesis, along with `methylfolate trap`.]. 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:16197314
;
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:NP232816.RAsUSipT1U2TmRg2yX68XdJh8AcDXpGtNJJHG8yGWYMV0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}