@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns
> .
@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:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_head
{
this:
np:hasAssertion
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_assertion
;
np:hasProvenance
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_provenance
;
np:hasPublicationInfo
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_assertion
a
np:Assertion
.
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_provenance
a
np:Provenance
.
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN5c260b8d2bae3ee5db554c17de0d9eee
sio:SIO_000628
miriam-gene:6647
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_provenance
{
dgn-np:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_assertion
dcterms:description
"[Because both IfRec and SOD-1 map to mouse chromosome 16, it will now be possible to use mice trisomic for this chromosome to determine whether certain aspects of the Down syndrome phenotype in man are caused by an altered dosage of IfRec and SOD-1.]. 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:6154946
;
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:NP1304898.RA00B9uogrLsDd8WXQAauSUFRnzo-oNUtfaDktzSgVMns130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:37+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" .
}