@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8
> .
@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:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_head
{
this:
np:hasAssertion
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_assertion
;
np:hasProvenance
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_assertion
a
np:Assertion
.
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_provenance
a
np:Provenance
.
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_assertion
{
miriam-gene:7433
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGN9e0a2e5467e199f4d3a4ed4ec8117cbb
sio:SIO_000628
miriam-gene:7433
,
lld:C0023890
;
a
sio:SIO_001121
.
}
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_provenance
{
dgn-np:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_assertion
dcterms:description
"[Conversely, the process of HVR1 sequence diversification, although differed considerably among patients, was stable over time and directly correlated with infections by HCV type 2, lower alanine aminotransferase (ALT) levels, and absence of cirrhosis.]. 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-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:NP881509.RAMzP-UBBiUqfpDSc-beC4DH31dv6fONZV6ALWDuNxVi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}