@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_head
{
this:
np:hasAssertion
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_assertion
;
np:hasProvenance
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_provenance
;
np:hasPublicationInfo
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_assertion
a
np:Assertion
.
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_provenance
a
np:Provenance
.
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_assertion
{
miriam-gene:5053
a
ncit:C16612
.
lld:C0751435
a
ncit:C7057
.
dgn-gda:DGNe8af934bd50817e2fcef7a53b4382c5d
sio:SIO_000628
miriam-gene:5053
,
lld:C0751435
;
a
sio:SIO_001121
.
}
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_provenance
{
dgn-np:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_assertion
dcterms:description
"[The aim of the study was to determine the mutations responsible for mild forms of HPA and to relate different clinical phenotypes of HPA patients to their PAH genotypes in order to better predict the clinical phenotype and implement optimal dietary therapy and prognosis in newborns with the disease.]. 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:23792259
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP606513.RA4Xnj0Ur3EisoO06ui8YmqNUI1h4xOrLd3PbVSihK4Ds130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:42+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}