@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA
> .
@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:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_head
{
this:
np:hasAssertion
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_assertion
;
np:hasProvenance
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_provenance
;
np:hasPublicationInfo
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_assertion
a
np:Assertion
.
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_provenance
a
np:Provenance
.
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_assertion
{
miriam-gene:760
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNecec26e578b43cf80ce37d9853f6c017
sio:SIO_000628
miriam-gene:760
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_provenance
{
dgn-np:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_assertion
dcterms:description
"[The presence of mental retardation and relative infrequency of skeletal fractures in our patients resembles the clinical course of patients with the Arabic mutation of the CA II gene, but this mutation was not found in our patients.]. 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:11795660
;
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:NP727043.RA3_Y1PwO6Fim9upu0ZWkiXG8jUzOSn8xDWmzwlf39GTA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}