@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA
> .
@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:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_head
{
this:
np:hasAssertion
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion
;
np:hasProvenance
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance
;
np:hasPublicationInfo
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion
a
np:Assertion
.
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance
a
np:Provenance
.
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGN70b908789d90192a40f2bb1c08c3814a
sio:SIO_000628
miriam-gene:6520
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance
{
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion
dcterms:description
"[In an attempt to determine the clonality of L & H cells and to clarify the link between NLPHD and complicating LCL, we used polymerase chain reaction (PCR) to analyze 33 cases of NLPHD, including 15 cases with simultaneous or subsequent LCL, for clonal immunoglobulin (lg) heavy chain variable region (VH) gene rearrangements.]. 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:8630407
;
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:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}