@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE
> .
@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:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_head
{
this:
np:hasAssertion
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion
;
np:hasProvenance
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion
a
np:Assertion
.
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance
a
np:Provenance
.
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion
{
miriam-gene:7167
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNfb72e3b48b3604f3d892398fb7044683
sio:SIO_000628
miriam-gene:7167
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance
{
dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion
dcterms:description
"[These novel results confirm the existence of a transport mechanism which permits transfer of active TPI from K562 cells to deficient cells, and may have important implications for developing different therapeutic approaches for TPI deficiency and other metabolic disorders of glycolysis.]. 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:9125215
;
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:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}