@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU
> .
@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:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_head
{
this:
np:hasAssertion
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_assertion
;
np:hasProvenance
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_provenance
;
np:hasPublicationInfo
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_assertion
a
np:Assertion
.
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_provenance
a
np:Provenance
.
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_assertion
{
miriam-gene:6948
a
ncit:C16612
.
lld:C0333006
a
ncit:C7057
.
dgn-gda:DGNb74596fd926d44e54bbf1c4275c80a2b
sio:SIO_000628
miriam-gene:6948
,
lld:C0333006
;
a
sio:SIO_001121
.
}
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_provenance
{
dgn-np:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_assertion
dcterms:description
"[Studies of the congenital deficiency TC II suggest the following: (1) The function of TC II is the promotion of cell uptake of physiologic amounts of Cbl, which can also be accomplished by very large amounts of Cbl, and not in any intracellular process.]. 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:7342493
;
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:NP768428.RAJI-s9xALtz6LqSww3GDYCjNmYW2mMKO-FxKx7ZC6XJU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}