@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY
> .
@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:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_head
{
this:
np:hasAssertion
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_assertion
;
np:hasProvenance
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_assertion
a
np:Assertion
.
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_provenance
a
np:Provenance
.
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN572e69c87a03b462a0f6b79e59b1dc54
sio:SIO_000628
miriam-gene:4524
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_provenance
{
dgn-np:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_assertion
dcterms:description
"[Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism, being a putative steatogenic factor, may promote liver fibrosis progression in patients with chronic hepatitis C. This study aimed to verify the role of recipient MTHFR polymorphism in favouring graft fibrosis progression in patients with recurrent HCV after orthotopic liver transplantation (OLT).]. 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:17900242
;
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:NP760955.RAf1gjj544S0cEMCXSitfymVDvvPFxAF-0k_3Qj_zgHFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}