@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y
> .
@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:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_head
{
this:
np:hasAssertion
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_assertion
;
np:hasProvenance
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_assertion
a
np:Assertion
.
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_provenance
a
np:Provenance
.
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_assertion
{
miriam-gene:57614
a
ncit:C16612
.
lld:C0410422
a
ncit:C7057
.
dgn-gda:DGNd0750f2275621c64c37c1f3887084c83
sio:SIO_000628
miriam-gene:57614
,
lld:C0410422
;
a
sio:SIO_001121
.
}
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_provenance
{
dgn-np:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_assertion
dcterms:description
"[Mutation screening in RANK and the genes PIGN and KIAA1468 led to detection of two variants (one in RANK and one in PIGN), which are in linkage disequilibrium with the rare D18S60 allele, but not independently associated with CRMO.]. 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:11973628
;
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:NP537438.RAJ4pJ8HbBbLkJ4UQtYO2iyQeobdIPNk6AeMhHl0G05-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}