@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA
> .
@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:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_head
{
this:
np:hasAssertion
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_assertion
;
np:hasProvenance
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_provenance
;
np:hasPublicationInfo
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_assertion
a
np:Assertion
.
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_provenance
a
np:Provenance
.
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_assertion
{
miriam-gene:4179
a
ncit:C16612
.
lld:C0022408
a
ncit:C7057
.
dgn-gda:DGN373acae45bfa0cf99f2fae95808aa9d8
sio:SIO_000628
miriam-gene:4179
,
lld:C0022408
;
a
sio:SIO_001121
.
}
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_provenance
{
dgn-np:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_assertion
dcterms:description
"[In view of the clinical similarities between polyarticular osteoarthritis (POA) with metacarpophalangeal (MCP) joint involvement and the arthropathy that occurs in hereditary haemochromatosis (HH), it was hypothesized that osteochondral damage in both disorders may be due to localized iron overload.]. 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:20560808
;
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:NP896627.RA0GRqiRvdEGKmeoJJ_v2wsIHBxlDkeh7BW2CU_WkwzJA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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" .
}