@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg
> .
@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:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_head
{
this:
np:hasAssertion
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_assertion
;
np:hasProvenance
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_provenance
;
np:hasPublicationInfo
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_assertion
a
np:Assertion
.
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_provenance
a
np:Provenance
.
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_assertion
{
miriam-gene:4069
a
ncit:C16612
.
lld:C0281479
a
ncit:C7057
.
dgn-gda:DGNfdacbaf231e84eb7daede948050016ae
sio:SIO_000628
miriam-gene:4069
,
lld:C0281479
;
a
sio:SIO_001121
.
}
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_provenance
{
dgn-np:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_assertion
dcterms:description
"[Two kindreds with hereditary systemic amyloidosis caused by the first two mutations to be described in the human lysozyme gene were discovered recently and study of the variant lysozyme has been powerfully informative about mechanisms of amyloid fibrillogenesis.]. 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:10534505
;
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:NP828087.RA4_SRHiPHedOdNqB7CzwxaWbdShzdQVwUpFYiY0PXmUg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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: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" .
}