@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_head
{
this:
np:hasAssertion
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_assertion
;
np:hasProvenance
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_assertion
a
np:Assertion
.
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_provenance
a
np:Provenance
.
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN0e7a2b9b101e941b192ab25700243965
sio:SIO_000628
miriam-gene:4548
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_provenance
{
dgn-np:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_assertion
dcterms:description
"[In conclusion, the MTHFR 677TTor 1298CC genotypes are much rarer in Africans than in Caucasians. The 677TT low frequency may be related to the high effect of this mutation on homocysteine metabolism in the environmental conditions of this African region.]. 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:12964809
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP79635.RAeTj0WD-nkbTxzowls6pZNis-iLNmPE6JZhzRYMePrxA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:23+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}