@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s
> .
@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:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_head
{
this:
np:hasAssertion
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion
;
np:hasProvenance
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance
;
np:hasPublicationInfo
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion
a
np:Assertion
.
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance
a
np:Provenance
.
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion
{
miriam-gene:10934
a
ncit:C16612
.
lld:C0272236
a
ncit:C7057
.
dgn-gda:DGN0131000e1d6158d3ec30c2e76467c1f7
sio:SIO_000628
miriam-gene:10934
,
lld:C0272236
;
a
sio:SIO_001121
.
}
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance
{
dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion
dcterms:description
"[The delineation of hyper-IgM syndromes made it possible to better define the mechanisms underlying the two major events of antibody maturation in humans, CSR and introduction of somatic hypermutation (SHM) in the variable region of immunoglobulins.]. 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:15661022
;
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:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}