@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y
> .
@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/v4.0.0/void/
> .
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_head
{
this:
np:hasAssertion
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_assertion
;
np:hasProvenance
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_assertion
a
np:Assertion
.
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_provenance
a
np:Provenance
.
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNf0099598638844c7eb3d1adfea0fcda7
sio:SIO_000628
miriam-gene:4524
,
lld:C0018784
;
a
sio:SIO_001122
.
}
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_provenance
{
dgn-np:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_assertion
dcterms:description
"[We suggest that this analysis of the MTHFR C677T mutation should be further investigated to establish the etiology of SSHL, and that the same analysis should be taken into account in those patients with high levels of homocysteine.]. 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:20798492
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP835331.RADO9lQSrURTpNtKr_UuXhO873cN3mriZcP4qUtsqGZ4Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:03+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}