@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4
> .
@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:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_head
{
this:
np:hasAssertion
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_assertion
;
np:hasProvenance
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_provenance
;
np:hasPublicationInfo
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_assertion
a
np:Assertion
.
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_provenance
a
np:Provenance
.
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_assertion
{
miriam-gene:83876
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN2556470b89b831432ffa187ec73b2d65
sio:SIO_000628
miriam-gene:83876
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_provenance
{
dgn-np:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_assertion
dcterms:description
"[These results indicate that the few mutations observed in the B29 gene in these patients do not induce structural abnormalities of the CD79b protein and thus do not account for its low surface expression in B-CLL.]. 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:10552962
;
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:NP451794.RAbB7iMUhhL48JFRqtFNv23M6UvXPI1LbOqX64OEWljq4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}