@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU
> .
@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:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_head
{
this:
np:hasAssertion
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion
;
np:hasProvenance
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion
a
np:Assertion
.
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance
a
np:Provenance
.
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion
{
miriam-gene:3388
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN817d532595f51887736edd63751fd12a
sio:SIO_000628
miriam-gene:3388
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance
{
dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion
dcterms:description
"[In a previous study' we showed that the ICR1 epimutation is not present in growth retarded patients with dysmorphisms not typical for SRS, but its role in the development of isolated growth restriction needed to be further elucidated.]. 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:18404973
;
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:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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: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" .
}