@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs
> .
@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:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_head
{
this:
np:hasAssertion
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_assertion
;
np:hasProvenance
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_provenance
;
np:hasPublicationInfo
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_assertion
a
np:Assertion
.
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_provenance
a
np:Provenance
.
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_assertion
{
miriam-gene:1326
a
ncit:C16612
.
lld:C0007120
a
ncit:C7057
.
dgn-gda:DGN2d4dce0b469e5055346fb06a9ad6f4d6
sio:SIO_000628
miriam-gene:1326
,
lld:C0007120
;
a
sio:SIO_001121
.
}
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_provenance
{
dgn-np:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_assertion
dcterms:description
"[By virtue of FISH analysis and the creation of a BAC/P1 genomic clone contig we have mapped 19 murine homologues of genes and nine EST groups from the region deleted in DiGeorge syndrome and found them to be linked on mouse chromosome 16.]. 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:9740669
;
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:NP829909.RABBNTMtVl4ykkOZHedmc6VpTnmRLfuhCTU5BVoohSUrs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}