@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc
> .
@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:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_head
{
this:
np:hasAssertion
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_assertion
;
np:hasProvenance
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_assertion
a
np:Assertion
.
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_provenance
a
np:Provenance
.
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_assertion
{
miriam-gene:7031
a
ncit:C16612
.
lld:C1854414
a
ncit:C7057
.
dgn-gda:DGNd8e7f2b8f6552564f14942fcbfc62183
sio:SIO_000628
miriam-gene:7031
,
lld:C1854414
;
a
sio:SIO_001121
.
}
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_provenance
{
dgn-np:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_assertion
dcterms:description
"[In order to identify candidate genes for Down syndrome phenotypes or monogenic disorders that map to human chromosome 21q22.3, we have used genomic sequence and expressed sequence tags mapping to an autosomal recessive deafness (DFNB10) critical region to isolate a novel 2.5-kb cDNA that maps between TFF1 and D21S49.]. 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:11281453
;
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:NP672604.RANstnEg1cQ_dmVPKlWT_mwIAD7LHeZyxmSMfW4GarWvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}