@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o
> .
@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:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_head
{
this:
np:hasAssertion
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_assertion
;
np:hasProvenance
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_assertion
a
np:Assertion
.
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_provenance
a
np:Provenance
.
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0812393
a
ncit:C7057
.
dgn-gda:DGN7e351fb5986580ff202fd1ac845b34ce
sio:SIO_000628
miriam-gene:4524
,
lld:C0812393
;
a
sio:SIO_001121
.
}
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_provenance
{
dgn-np:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_assertion
dcterms:description
"[A common C677T polymorphism in MTHFR has been associated with an increased risk for the development of cardiovascular disease, Alzheimer's disease, and depression in adults, and of neural tube defects in the fetus.]. 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:23116396
;
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:NP449876.RAs5kgo48L2PPWqrEXz7WZD6P84COS60lZGaR219zqd0o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}