@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4
> .
@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:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_head
{
this:
np:hasAssertion
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_assertion
;
np:hasProvenance
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_provenance
;
np:hasPublicationInfo
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_assertion
a
np:Assertion
.
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_provenance
a
np:Provenance
.
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_assertion
{
miriam-gene:118429
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGNe453bd43449dc7bfc6b9a4a617c5564b
sio:SIO_000628
miriam-gene:118429
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_provenance
{
dgn-np:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_assertion
dcterms:description
"[Seven cases of chromosomal aberrations observed with ISH (three for monosomy and four for trisomy) were confirmed by this classical cytogenetic technique, whereas in five instances an aberration was found only with ISH (twice for monosomy, twice for trisomy, and one disomy for the Y-probe).]. 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:2004382
;
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:NP548084.RAL8KkZKdPw1mQx2LhFEtv7qwfGxqON3XTR_5FTZU2_R4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}