@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs
> .
@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:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_head
{
this:
np:hasAssertion
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_assertion
;
np:hasProvenance
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_provenance
;
np:hasPublicationInfo
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_assertion
a
np:Assertion
.
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_provenance
a
np:Provenance
.
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_assertion
{
miriam-gene:8718
a
ncit:C16612
.
lld:C0035439
a
ncit:C7057
.
dgn-gda:DGN3b371b7e163d32ead666e2237542dcab
sio:SIO_000628
miriam-gene:8718
,
lld:C0035439
;
a
sio:SIO_001121
.
}
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_provenance
{
dgn-np:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_assertion
dcterms:description
"[The results are consistent with the hypothesis that susceptibility to RHD is genetically linked, and this in turn may be associated mainly with HLA class II antigens and weakly with class I antigens, with DR3, DR7, and B16 influencing susceptibility and DR5 conferring protection.]. 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:8504512
;
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:NP612724.RAWzd0HaqfiGl6Et_YFsbxdbCxdo8zrQO2xgYa0Mnk9Bs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}