@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE
> .
@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:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_head
{
this:
np:hasAssertion
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_assertion
;
np:hasProvenance
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_provenance
;
np:hasPublicationInfo
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_assertion
a
np:Assertion
.
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_provenance
a
np:Provenance
.
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C0025958
a
ncit:C7057
.
dgn-gda:DGN7ca65e63082b90a9effe4aa167aba4d1
sio:SIO_000628
miriam-gene:668
,
lld:C0025958
;
a
sio:SIO_001121
.
}
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_provenance
{
dgn-np:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_assertion
dcterms:description
"[Almost all cases with interstitial deletions containing 3q23 have not only BPES but also microcephaly and developmental retardation, while those without deletions, including those with apparently balanced translocations, only have BPES.]. 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:8256811
;
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:NP325592.RAwViVNAOjEGvBW5qEYcFV3vGPsQ-hkiqdT6fYrHNIxdE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}