@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA
> .
@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:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_head
{
this:
np:hasAssertion
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion
;
np:hasProvenance
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance
;
np:hasPublicationInfo
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion
a
np:Assertion
.
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance
a
np:Provenance
.
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion
{
miriam-gene:389421
a
ncit:C16612
.
lld:C0034012
a
ncit:C7057
.
dgn-gda:DGNe4730dcddb3d0b2a114caf4cb4ada612
sio:SIO_000628
miriam-gene:389421
,
lld:C0034012
;
a
sio:SIO_001122
.
}
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance
{
dgn-np:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion
dcterms:description
"[Our results show that mutations in the coding region or 3 untranslated region miRNA recognition elements A and B of LIN28B do not underlie CDGP. Lack of any variation in the coding region of the gene suggests that LIN28B in developmental timing is so crucial that any changes in the conserved protein would probably be lethal.]. 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:20350940
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:43+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" .
}