@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw
> .
@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:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_head
{
this:
np:hasAssertion
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_assertion
;
np:hasProvenance
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_provenance
;
np:hasPublicationInfo
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_assertion
a
np:Assertion
.
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_provenance
a
np:Provenance
.
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0349632
a
ncit:C7057
.
dgn-gda:DGNc8b98d9be439e50d606d49422f6e5794
sio:SIO_000628
miriam-gene:6520
,
lld:C0349632
;
a
sio:SIO_001121
.
}
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_provenance
{
dgn-np:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_assertion
dcterms:description
"[An investigation of VH genes used in five typical cases of SLVL has shown somatic hypermutation from germline sequences in all cases, indicating that the cell of origin has been exposed to the hypermutation mechanism.]. 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:7888678
;
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:NP918831.RAjPyV4ZUuFKsDxnCWh8xZVlAigGalHcOfInVBaolGzJw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}