@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo
> .
@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:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_head
{
this:
np:hasAssertion
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_assertion
;
np:hasProvenance
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_assertion
a
np:Assertion
.
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_provenance
a
np:Provenance
.
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_assertion
{
miriam-gene:2317
a
ncit:C16612
.
lld:C0175778
a
ncit:C7057
.
dgn-gda:DGN5a2c4bec0bdd00b43a797639ba32a879
sio:SIO_000628
miriam-gene:2317
,
lld:C0175778
;
a
sio:SIO_001121
.
}
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_provenance
{
dgn-np:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_assertion
dcterms:description
"[The clinical and radiographic pattern (joint dislocations, vertebral changes, normal carpal age, lack of facial flattening, and recessive inheritance) is characteristic and distinguishes CHST3 deficiency from other disorders with congenital dislocations such as filamin B-associated dominant Larsen syndrome and Desbuquois syndrome.]. 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:20830804
;
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:NP924364.RAIyR7YdUmFgrLpI-CWmiPawDqOxUU8pAHZYoPhSP5uPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}