@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc
> .
@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:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_head
{
this:
np:hasAssertion
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_assertion
;
np:hasProvenance
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_assertion
a
np:Assertion
.
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_provenance
a
np:Provenance
.
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_assertion
{
miriam-gene:8163
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN10479f592dfaa6be101362fb03b323e3
sio:SIO_000628
miriam-gene:8163
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_provenance
{
dgn-np:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_assertion
dcterms:description
"[The sequences of the complementarity determining region (CDR)3 on T-cell receptor expressing Vbeta5.1 were examined in six patients with chronic hepatitis C. The sequences were similar to each other and all had one common amino acid (valine) irrespective of different HLA haplotype.]. 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:9075650
;
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:NP319463.RAavqrpr4Rvm3L4szjpofOsFNrLs6-aHeF836uVrDOHAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}