@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU
> .
@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:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_head
{
this:
np:hasAssertion
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_assertion
;
np:hasProvenance
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_provenance
;
np:hasPublicationInfo
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_assertion
a
np:Assertion
.
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_provenance
a
np:Provenance
.
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_assertion
{
miriam-gene:56731
a
ncit:C16612
.
lld:C0175701
a
ncit:C7057
.
dgn-gda:DGN651e09c66d721902802e563fe826e032
sio:SIO_000628
miriam-gene:56731
,
lld:C0175701
;
a
sio:SIO_001121
.
}
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_provenance
{
dgn-np:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_assertion
dcterms:description
"[We previously demonstrated that FGD1, the Cdc42 guanine nucleotide exchange factor (GEF) responsible for faciogenital dysplasia, and its homologue FGD3 are targeted by the ubiquitin ligase SCF(FWD1) upon phosphorylation of two serine residues in their DSGIDS motif and subsequently degraded by the proteasome.]. 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:20045932
;
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:NP777368.RAUeWI-h-q0Zgz9OtqII8DANSswFNpZnCEZYKeEiaOvQU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}