@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ
> .
@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:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_head
{
this:
np:hasAssertion
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_assertion
;
np:hasProvenance
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_assertion
a
np:Assertion
.
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_provenance
a
np:Provenance
.
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_assertion
{
miriam-gene:1109
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNe8182979afb5277be2ca95bfebe32316
sio:SIO_000628
miriam-gene:1109
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_provenance
{
dgn-np:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_assertion
dcterms:description
"[We observe first that no statistical test is able to identify selection in the CDR antigen-binding sites, second that tests can reliably detect selection in the FR and third that antibodies from nasal biopsies from patients with Wegener's granulomatosis and pathogenic antibodies from systemic lupus erythematosus do not appear to be as stringently selected for structural integrity as other groups of functional sequences.]. 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:20501523
;
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:NP756966.RALsmZJupPld4IgUnwjj4jZ3NZy-41payzxYrc3SD15iQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}