@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY
> .
@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:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_head
{
this:
np:hasAssertion
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion
;
np:hasProvenance
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance
;
np:hasPublicationInfo
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion
a
np:Assertion
.
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance
a
np:Provenance
.
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN8cf9e1978b48df7e5f89f855efe5865d
sio:SIO_000628
miriam-gene:4709
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance
{
dgn-np:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion
dcterms:description
"[Some of these gene products are specifically dedicated to B(12) transport, whereas others embrace additional roles, which explains the heterogeneity in the clinical picture of the many genetic disorders causing B(12) deficiency.]. 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:22547309
;
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:NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}