@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_head
{
this:
np:hasAssertion
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_assertion
;
np:hasProvenance
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_assertion
a
np:Assertion
.
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_provenance
a
np:Provenance
.
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_assertion
{
miriam-gene:1436
a
ncit:C16612
.
lld:C3711381
a
ncit:C7057
.
dgn-gda:DGN3f9483e84037b63bd44c0ae61977fa6d
sio:SIO_000628
miriam-gene:1436
,
lld:C3711381
;
a
sio:SIO_001121
.
}
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_provenance
{
dgn-np:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_assertion
dcterms:description
"[To the best of our knowledge, this is the first documented ALSP-linked CSF1R mutation in Korea and supports the suggestion that HDLS and POLD, with pathological characteristics that are somewhat different but which are caused by CSF1R mutations, are the same spectrum of disease, ALSP.]. 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:25563800
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1253421.RAXpt9ZAmjX5uRaHI3zAi7b7EehCJ5Bf0IYwuVs5kmmVQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:14+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}