@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4
> .
@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:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_head
{
this:
np:hasAssertion
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_assertion
;
np:hasProvenance
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_provenance
;
np:hasPublicationInfo
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_assertion
a
np:Assertion
.
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_provenance
a
np:Provenance
.
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_assertion
{
miriam-gene:5053
a
ncit:C16612
.
lld:C0751434
a
ncit:C7057
.
dgn-gda:DGN2b05032bcc8f208509f28f7e692feac2
sio:SIO_000628
miriam-gene:5053
,
lld:C0751434
;
a
sio:SIO_001121
.
}
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_provenance
{
dgn-np:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_assertion
dcterms:description
"[Out of a population of 138,598 infants born in southern Poland between 1987 and 1989, and screened for phenylketonuria (PKU), 28 cases were ascertained probands and their parents were isolated and eight polymorphic restriction sites were analyzed within the phenylalanine hydroxylase gene region.]. 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:1671770
;
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:NP183793.RAfG6ZTXWEa1wKmJ1caij6DQE_NNs-obEcMhDCbHRT4L4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}