@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA
> .
@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:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_head
{
this:
np:hasAssertion
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_assertion
;
np:hasProvenance
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_provenance
;
np:hasPublicationInfo
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_assertion
a
np:Assertion
.
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_provenance
a
np:Provenance
.
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_assertion
{
miriam-gene:1154
a
ncit:C16612
.
lld:C0027960
a
ncit:C7057
.
dgn-gda:DGN0aa44cbfe21ed1ccd9cf95c28805b718
sio:SIO_000628
miriam-gene:1154
,
lld:C0027960
;
a
sio:SIO_001121
.
}
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_provenance
{
dgn-np:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_assertion
dcterms:description
"[In this study, the frequency of heterozygous XY complete mole in 93 consecutive cases of histologically proven complete moles managed in Hong Kong was assessed by the technique of chromosome in situ hybridization (CISH) using DNA probes specific for the short arm of the Y chromosome.]. 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:7835778
;
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:NP921305.RAw6AKdbxbX-NhE7_uUZgF7PlFyaLDcKbEu6_iuXjWRXA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}