@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k
> .
@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:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_head
{
this:
np:hasAssertion
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_assertion
;
np:hasProvenance
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_provenance
;
np:hasPublicationInfo
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_assertion
a
np:Assertion
.
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_provenance
a
np:Provenance
.
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0302809
a
ncit:C7057
.
dgn-gda:DGN4ba7bc1cd859892b6457d288a9571b83
sio:SIO_000628
miriam-gene:2147
,
lld:C0302809
;
a
sio:SIO_001121
.
}
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_provenance
{
dgn-np:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_assertion
dcterms:description
"[Analyzing the full-length sequences of 28 genotype-4 and 11 genotype-3 HEV retrievable from DNA databases and 35 partial sequences recovered from patients with acute or fulminant hepatitis, we show that the presence of both U3148 and C5907 is associated with fulminant hepatitis in patients with HEV of genotype 4 (p = 0.0042) and genotype 3 or 4 (p = 0.0009), and that the prothrombin activity is significantly lower in patients infected with HEV carrying U3148 and C5907 than in those without the substitutions (p = 0.0069).]. 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:19638731
;
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:NP754028.RA356v139r4MN2_hX0B6Pb5pU0_LAAt3WXmMVgqzQJl3k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:27+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
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;
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" .
}