@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54
> .
@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:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_head
{
this:
np:hasAssertion
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion
;
np:hasProvenance
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_provenance
;
np:hasPublicationInfo
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion
a
np:Assertion
.
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_provenance
a
np:Provenance
.
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion
{
miriam-gene:2261
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN8b279b99d54ca44add32ac81213d49d8
sio:SIO_000628
miriam-gene:2261
,
lld:C0000768
;
a
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.
}
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_provenance
{
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion
dcterms:description
"[The number of birth defect cases in the Texas Birth Defects Registry (one of the largest active birth defects surveillance systems in the world) enabled us to examine six different heritable disorders (aqueductal stenosis, infantile polycystic kidney disease, achondroplasia, thanatophoric dwarfism, chondrodysplasia/dwarfism not otherwise specified (NOS), and osteogenesis imperfecta) for a variety of descriptive demographic variables.]. 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:22102535
;
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:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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
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pav:authoredBy
<
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> , <
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
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pav:version
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}