@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4
> .
@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:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_head
{
this:
np:hasAssertion
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_assertion
;
np:hasProvenance
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_provenance
;
np:hasPublicationInfo
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_assertion
a
np:Assertion
.
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_provenance
a
np:Provenance
.
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0023234
a
ncit:C7057
.
dgn-gda:DGN3dc216d18698a25f2f86ee10f91d0fdd
sio:SIO_000628
miriam-gene:5660
,
lld:C0023234
;
a
sio:SIO_001121
.
}
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_provenance
{
dgn-np:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_assertion
dcterms:description
"[The eleven probands who had familial protein-C deficiency were more likely to have early onset of Legg-Perthes disease (at or before the age of five years) than the eleven children who had normal levels of protein C, protein S, and lipoprotein(a) as well as normal fibrinolytic activity (chi-square = 6.6; p = 0.01).]. 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:8550676
;
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:NP696560.RAVNuYLQF68XDcEmaoQXp34KZqndoUvwwUWKCCpzJIK_4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}