@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc
> .
@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:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_head
{
this:
np:hasAssertion
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_assertion
;
np:hasProvenance
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_assertion
a
np:Assertion
.
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_provenance
a
np:Provenance
.
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_assertion
{
miriam-gene:7035
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGNb759390745bf5ed87fc869f68a9b5227
sio:SIO_000628
miriam-gene:7035
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_provenance
{
dgn-np:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_assertion
dcterms:description
"[Although not yet completely understood, SRS and BWS can be used as models to decipher the functional link between the observed (epi)genetic mutations and the clinical features in individuals with disturbed growth.]. 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:19407494
;
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:NP735894.RAXgyYMEzN9dnm5FG-fEjPBQFAKYbkFeFlvKPFE5AVvLc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:18+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" .
}