@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs
> .
@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:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_head
{
this:
np:hasAssertion
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_assertion
;
np:hasProvenance
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_provenance
;
np:hasPublicationInfo
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_assertion
a
np:Assertion
.
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_provenance
a
np:Provenance
.
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0011991
a
ncit:C7057
.
dgn-gda:DGNd3b69b8a81fb4061bf2410790c0f8d70
sio:SIO_000628
miriam-gene:1956
,
lld:C0011991
;
a
sio:SIO_001121
.
}
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_provenance
{
dgn-np:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_assertion
dcterms:description
"[In an attempt to identify the gene causative for SD, we studied several functional candidate genes, based on their implication in overlapping phenotypes in mice (EGFR) or in humans (HRAS, JUP, DSP EPPK1, PLEC1, and CTNNB1) in 8 patients affected by SD.]. 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:19322062
;
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:NP394458.RA9P1TiFRnelvKObfBkBxgfsi2r2kMsEuRM_S3s3ZM2Cs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}