@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI
> .
@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:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_head
{
this:
np:hasAssertion
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion
;
np:hasProvenance
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance
;
np:hasPublicationInfo
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion
a
np:Assertion
.
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance
a
np:Provenance
.
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C3495426
a
ncit:C7057
.
dgn-gda:DGN3d1ac43b35aa561eb4f506a363149e75
sio:SIO_000628
miriam-gene:4709
,
lld:C3495426
;
a
sio:SIO_001121
.
}
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance
{
dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion
dcterms:description
"[Plasma Hcy levels, MTHFR gene mutation, red blood cell (RBC) folate and vitamin B12 serum levels were measured in all subjects.Results: No significant differences were observed neither in plasma Hcy levels, RBC folate and vitamin B12 serum levels nor in the prevalence of homozygous and heterozygous MTHFR gene mutation between the two groups studied.Conclusions: In the present study RM is not associated with hyperhomocysteinemia, and/or the MTHFR gene mutation.]. 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:23095199
;
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:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}