@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_provenance
a
np:Provenance
.
dgn-np:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:260402
a
ncit:C16612
.
lld:C0036439
a
ncit:C7057
.
dgn-gda:DGN8561dd14b037aed7daa3cc4c9ce356d6
sio:SIO_000628
miriam-gene:260402
,
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;
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.
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dgn-np:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_provenance
{
dgn-np:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_assertion
dcterms:description
"[Our objectives were to quantify the genetic effect in AIS, determine the expressivity and penetrance of AIS in large family groupings, and examine larger scoliosis pedigrees for evidence of multiple genes.]. 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:16540873
;
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:NP299626.RAQ6KQ7zLd08Rf0_VjnKLIY3pYDtXlrPC4JRk2kbN3zT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
}