@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY
> .
@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:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_head
{
this:
np:hasAssertion
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_assertion
;
np:hasProvenance
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_provenance
;
np:hasPublicationInfo
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_assertion
a
np:Assertion
.
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_provenance
a
np:Provenance
.
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_assertion
{
miriam-gene:4810
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNb9781d7a0b0ef51d746f70172c188c4b
sio:SIO_000628
miriam-gene:4810
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_provenance
{
dgn-np:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_assertion
dcterms:description
"[The association of genetic variation in the SHMT1 gene, alone and in interaction with MTHFR, in relation to CVD risk is relatively understudied at the population level and results in the NHS confirmed a past report of gene-gene interaction, which is consistent with mechanisms suggested by basic science studies.]. 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:21178087
;
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:NP414242.RA9hzY1f_NycbSBcROCXw7woIfVkgeeGm4QDO-e9pB_PY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}