@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ
> .
@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:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_head
{
this:
np:hasAssertion
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_assertion
;
np:hasProvenance
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_assertion
a
np:Assertion
.
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_provenance
a
np:Provenance
.
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_assertion
{
miriam-gene:7433
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGNd2a376fc78110332789dba69f7e97c92
sio:SIO_000628
miriam-gene:7433
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_provenance
{
dgn-np:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_assertion
dcterms:description
"[Our findings indicate that HVR1 variation has an adaptive significance and is associated with favorable features of liver disease and suggest that prospective, rather than static, observations are required to model the process of HCV variation.]. 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:9620342
;
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:NP1396969.RAXmY4z8C-M4ySPtXJnH3D1qAlecQ28nBJAMyyNSP1rFQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:19+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" .
}