@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o
> .
@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:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_head
{
this:
np:hasAssertion
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_assertion
;
np:hasProvenance
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_assertion
a
np:Assertion
.
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_provenance
a
np:Provenance
.
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_assertion
{
miriam-gene:7538
a
ncit:C16612
.
lld:C1848533
a
ncit:C7057
.
dgn-gda:DGN9557fd6ace2a6fe04033c3e7ed57d5f1
sio:SIO_000628
miriam-gene:7538
,
lld:C1848533
;
a
sio:SIO_001121
.
}
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_provenance
{
dgn-np:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_assertion
dcterms:description
"[These findings suggest the possibility that the AVED syndrome may not arise from an inability of TTP to bind or to transfer alpha tocopherol, but rather from defects in other activities of the protein.]. 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:15065857
;
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:NP842608.RAKe7ClX7D2bDUDdvUiqDPafmUXTgsZmRWfK0Puv3tD3o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}