@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE
> .
@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:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_head
{
this:
np:hasAssertion
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_assertion
;
np:hasProvenance
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_provenance
;
np:hasPublicationInfo
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_assertion
a
np:Assertion
.
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_provenance
a
np:Provenance
.
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0035078
a
ncit:C7057
.
dgn-gda:DGN2dcadd4a18febf23b6fcd1e4229d544a
sio:SIO_000628
miriam-gene:4524
,
lld:C0035078
;
a
sio:SIO_001121
.
}
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_provenance
{
dgn-np:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_assertion
dcterms:description
"[These findings provide additional support for the hypothesis that the mutant TT genotype at nucleotide 677 of the gene regulating MTHFR activity may increase the mortality risk in patients with ESRD.]. 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:19272686
;
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:NP448688.RAA6fT7pxa29OStXDveXl_sK9SPwXZuykVOtPLO8Qc0QE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}