@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM
> .
@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:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_head
{
this:
np:hasAssertion
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_assertion
;
np:hasProvenance
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_provenance
;
np:hasPublicationInfo
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_assertion
a
np:Assertion
.
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_provenance
a
np:Provenance
.
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN593175fcaaf26e7dbdc16635629a10a5
sio:SIO_000628
miriam-gene:613
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_provenance
{
dgn-np:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_assertion
dcterms:description
"[ Sequence polymorphisms were found in the 5' promotor region of BCR gene, most of them being SNPs. No relativity can be validated between the SNPs and the disease. But it appears that some SNPs might have the probability of bringing influence to the trans]. 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:15248918
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP86714.RAAvMDSeg32PHb2NHZzESApDV7Xilmwc3uNwshhmo5HTM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:27+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" .
}