@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc
> .
@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:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_head
{
this:
np:hasAssertion
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_assertion
;
np:hasProvenance
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_provenance
;
np:hasPublicationInfo
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_assertion
a
np:Assertion
.
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_provenance
a
np:Provenance
.
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_assertion
{
miriam-gene:871
a
ncit:C16612
.
lld:C0029434
a
ncit:C7057
.
dgn-gda:DGNb99610f16533de6e1757c4b36644435b
sio:SIO_000628
miriam-gene:871
,
lld:C0029434
;
a
sio:SIO_001121
.
}
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_provenance
{
dgn-np:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_assertion
dcterms:description
"[Since then, an additional putative collagen chaperone complex, composed of FKBP10 (also known as FKBP65) and SERPINH1 (also known as HSP47), also has been shown to be mutated in recessive OI.]. 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:20839288
;
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:NP935803.RAXsHquIqZZnfiEyocFxg34k-bmw3k67gx5R5LBTAs_bc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:33+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" .
}