@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY
> .
@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:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_head
{
this:
np:hasAssertion
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_assertion
;
np:hasProvenance
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_provenance
;
np:hasPublicationInfo
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_assertion
a
np:Assertion
.
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_provenance
a
np:Provenance
.
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0042847
a
ncit:C7057
.
dgn-gda:DGN48db984b6021a72e914e44f1178d39e8
sio:SIO_000628
miriam-gene:4524
,
lld:C0042847
;
a
sio:SIO_001121
.
}
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_provenance
{
dgn-np:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_assertion
dcterms:description
"[One of the plausible reasons for susceptibility of individuals with MTHFR C677T in the studied population to various disorders is the high frequency of hyperhomocysteinemia and vitamin B12 deficiency in the 'healthy population'.]. 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:21878957
;
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:NP709985.RARch7Eakbu5SYZTfzqKREsvmyttwW_F8E_9RacjQeQAY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}