@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods
> .
@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:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_head
{
this:
np:hasAssertion
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_assertion
;
np:hasProvenance
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_provenance
;
np:hasPublicationInfo
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_assertion
a
np:Assertion
.
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_provenance
a
np:Provenance
.
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_assertion
{
miriam-gene:5479
a
ncit:C16612
.
lld:C0029434
a
ncit:C7057
.
dgn-gda:DGNf4ad74bb8d7fa10f8aa671cd209dc5d2
sio:SIO_000628
miriam-gene:5479
,
lld:C0029434
;
a
sio:SIO_001121
.
}
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_provenance
{
dgn-np:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_assertion
dcterms:description
"[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered 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:21829228
;
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:NP523083.RATwe2e8CmJHKGVgQoqsvHhgG5NoV5nmLQrkx7qATFods130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:11+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" .
}