@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8
> .
@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:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_head
{
this:
np:hasAssertion
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_assertion
;
np:hasProvenance
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_provenance
;
np:hasPublicationInfo
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_assertion
a
np:Assertion
.
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_provenance
a
np:Provenance
.
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_assertion
{
miriam-gene:27152
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNc2cbea28766d4a54e58c5a507b608158
sio:SIO_000628
miriam-gene:27152
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_provenance
{
dgn-np:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_assertion
dcterms:description
"[The present study shows that the INT at first trimester was the only prenatal finding for the fetus with del(18p) syndrome and that molecular cytogenetic methods are useful for detecting chromosomal aberrations precisely.]. 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:15057945
;
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:NP747937.RAH7T3pxhmfQpyfJ1cXE2Au6Av1M7DE7CweYiVtnKoiW8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}