@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc
> .
@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:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_head
{
this:
np:hasAssertion
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion
;
np:hasProvenance
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance
;
np:hasPublicationInfo
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion
a
np:Assertion
.
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance
a
np:Provenance
.
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion
{
miriam-gene:862
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNd46ef041da225630b951712a918c0dbd
sio:SIO_000628
miriam-gene:862
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance
{
dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion
dcterms:description
"[Patient specific oligonucleotide primers were designed based on the complementarity determining regions (CDR) of each MM Ig sequence and used to amplify DNA by polymerase chain reaction for the detection of malignant cells.]. 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:7524734
;
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:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}