@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM
> .
@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:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_head
{
this:
np:hasAssertion
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_assertion
;
np:hasProvenance
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_assertion
a
np:Assertion
.
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_provenance
a
np:Provenance
.
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_assertion
{
miriam-gene:2133
a
ncit:C16612
.
lld:C1832588
a
ncit:C7057
.
dgn-gda:DGN124a4a367260beded8dd0e54798f51b9
sio:SIO_000628
miriam-gene:2133
,
lld:C1832588
;
a
sio:SIO_001121
.
}
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_provenance
{
dgn-np:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_assertion
dcterms:description
"[The proximal short arm of chromosome 11 harbors several candidate genes that could explain the patient's signs and symptoms including ALX4 and EXT2, which are always present in the interstitial deletion of the short arm of chromosome 11 in PSS.]. 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:17290930
;
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:NP593155.RA0yVWTKLf1u1sQleNNdj8okwFN4-aM9HQ3zWhMaaZLYM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:14+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" .
}