@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY
> .
@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/v4.0.0/void/
> .
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_head
{
this:
np:hasAssertion
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_assertion
;
np:hasProvenance
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_assertion
a
np:Assertion
.
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_provenance
a
np:Provenance
.
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_assertion
{
miriam-gene:11146
a
ncit:C16612
.
lld:C0332887
a
ncit:C7057
.
dgn-gda:DGNa0d68415b6eeb047d2fb68fe88fdc0c1
sio:SIO_000628
miriam-gene:11146
,
lld:C0332887
;
a
sio:SIO_001121
.
}
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_provenance
{
dgn-np:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_assertion
dcterms:description
"[Genotypes of nine family members were subsequently correlated with the presence or absence of congenital hypertrophy of the retinal pigment epithelium (CHRPE), since expression of this common extracolonic manifestation of FAP is largely determined by the length of the truncated protein.]. 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:8733048
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1354555.RAoO3-Hlfd2rzVJml7Wv2_P4BpDi82yrmMEoNbsEe1qsY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:00+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}