@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg
> .
@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:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_head
{
this:
np:hasAssertion
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_assertion
;
np:hasProvenance
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_provenance
;
np:hasPublicationInfo
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_assertion
a
np:Assertion
.
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_provenance
a
np:Provenance
.
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNb9664c70980bc45e3f0e490f65f108cd
sio:SIO_000628
miriam-gene:4524
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_provenance
{
dgn-np:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_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-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:NP816341.RA3WwszWpBaZ72nQRaWAutW9Ffa0PzA8jLwophzhADPdg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}