@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU
> .
@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:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_head
{
this:
np:hasAssertion
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_assertion
;
np:hasProvenance
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_provenance
;
np:hasPublicationInfo
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_assertion
a
np:Assertion
.
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_provenance
a
np:Provenance
.
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0025521
a
ncit:C7057
.
dgn-gda:DGN44512ad160eebabf65b709a6b92af86a
sio:SIO_000628
miriam-gene:4709
,
lld:C0025521
;
a
sio:SIO_001121
.
}
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_provenance
{
dgn-np:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_assertion
dcterms:description
"[As a consequence of investigations on the pathogenesis of an inborn error of metabolism characterized by increased urinary and plasma levels of methylmalonic acid, the metabolism of vitamin B12 and its functional roles have become elucidated.]. 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:7447389
;
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:NP463152.RAqqpdtvhkqsdwhuCrQd5ltb8Inuy1UTomqjHweG9XaLU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}