@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM
> .
@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:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_head
{
this:
np:hasAssertion
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_assertion
;
np:hasProvenance
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_assertion
a
np:Assertion
.
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_provenance
a
np:Provenance
.
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0795851
a
ncit:C7057
.
dgn-gda:DGN7dbb6ad1ec59ff08d7084be0157e9e29
sio:SIO_000628
miriam-gene:7389
,
lld:C0795851
;
a
sio:SIO_001121
.
}
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_provenance
{
dgn-np:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_assertion
dcterms:description
"[Our study, in conjunction with a prior study of UPD 14 and partial trisomy 14 cases, and what is known of imprinting in regions of mouse chromosomes homologous to human chromosome 14, leads us to conclude that 14q23-q32 is likely an area where imprinted genes may reside.]. 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:10951461
;
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:NP247251.RAFA9NWhBzPTaBQMzevWZtVmrvqiRGCfDQtfF9tBmkbcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}