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April 23, 2019 13:46
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@prefix nanopub: <http://www.nanopub.org/nschema#> . | |
@prefix dcterms: <http://purl.org/dc/terms/> . | |
@prefix opm: <http://purl.org/net/opmv/ns#> . | |
@prefix pav: <http://swan.mindinformatics.org/ontologies/1.2/pav/> . | |
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . | |
@prefix sio: <http://semanticscience.org/resource/> . | |
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> . | |
@prefix : <http://rdf.biosemantics.org/vocabularies/gene_disease_nanopub_example#> . | |
:NanoPub_1_Head { | |
: a nanopub:Nanopublication ; | |
nanopub:hasAssertion :NanoPub_1_Assertion ; | |
nanopub:hasProvenance :NanoPub_1_Provenance ; | |
nanopub:hasPublicationInfo :NanoPub_1_Pubinfo . | |
} | |
:NanoPub_1_Assertion { | |
:Association_1 a sio:statistical-association ; | |
sio:has-measurement-value :Association_1_p_value ; | |
sio:refers-to <http://bio2rdf.org/geneid:55835>, <http://bio2rdf.org/omim:210600> ; | |
rdfs:comment "This association has p-value of 0.00066, has attribute gene CENPJ (Entrenz gene id 55835) | |
and attribute disease Seckel Syndrome (OMIM 210600)."@en . | |
:Association_1_p_value a sio:probability-value ; | |
sio:has-value "0.0000656211037469712"^^xsd:float . | |
} | |
:NanoPub_1_Provenance { | |
:NanoPub_1_Assertion opm:wasDerivedFrom <http://rdf.biosemantics.org/vocabularies/text_mining/gene_disease_concept_profiles_1980_2010> ; | |
opm:wasGeneratedBy <http://rdf.biosemantics.org/vocabularies/text_mining/gene_disease_concept_profiles_matching_1980_2010> . | |
} | |
:NanoPub_1_Pubinfo { | |
: pav:authoredBy <http://www.researcherid.com/rid/B-6035-2012> , | |
<http://www.researcherid.com/rid/B-5927-2012> . | |
: pav:createdBy <http://www.researcherid.com/rid/B-5852-2012> ; | |
dcterms:created "2012-03-28T11:32:30.758274Z"^^xsd:dateTime ; | |
dcterms:rights <http://creativecommons.org/licenses/by/3.0/> ; | |
dcterms:rightsHolder <http://biosemantics.org> . | |
} |
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