@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U
> .
@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:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_head
{
this:
np:hasAssertion
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_assertion
;
np:hasProvenance
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_provenance
;
np:hasPublicationInfo
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_assertion
a
np:Assertion
.
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_provenance
a
np:Provenance
.
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_assertion
{
miriam-gene:3065
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN2f909fbcaaa9beb49fb45ea98e0a6b9e
sio:SIO_000628
miriam-gene:3065
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_provenance
{
dgn-np:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_assertion
dcterms:description
"[Recognition of and testing for HDL2 is important in South Africa's large Black population, and HD testing services cannot be considered complete unless testing for both HD1 and HDL2 are undertaken.]. 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:21838519
;
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:NP548532.RAtodVUGGoE1sWP251UAtHqY42bw05w-TI7CpbOWSL50U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}