@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo
> .
@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/v3.0.0/void/
> .
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_head
{
this:
np:hasAssertion
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_assertion
;
np:hasProvenance
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_assertion
a
np:Assertion
.
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_provenance
a
np:Provenance
.
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_assertion
{
miriam-gene:138428
a
ncit:C16612
.
lld:C0751265
a
ncit:C7057
.
dgn-gda:DGN2f723fb91e457d11ca98c87d757b022e
sio:SIO_000628
miriam-gene:138428
,
lld:C0751265
;
a
sio:SIO_001121
.
}
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_provenance
{
dgn-np:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_assertion
dcterms:description
"[Because of the timing for onset of symptomatic hypocalcemia, it was presumed that the patient had anticonvulsant-induced hypocalcemia, and he carried that diagnosis for 18 yr. Chromosome 22q11 deletion syndrome was first suspected at age 32 yr, based on the findings of subtle dysmorphic facial features and a history of learning disability in a patient with PTH-deficient hypocalcemia.]. 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:15472168
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP972590.RAnK7AI6sj7mlfxxmbEtomcGwgvQIu0Gc4QUyVfnpwXgo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:34+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}