@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ
> .
@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:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_head
{
this:
np:hasAssertion
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_assertion
;
np:hasProvenance
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_assertion
a
np:Assertion
.
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_provenance
a
np:Provenance
.
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_assertion
{
miriam-gene:1121
a
ncit:C16612
.
lld:C0678213
a
ncit:C7057
.
dgn-gda:DGN0b6c1328d164a0e26d0fecc00e38dfca
sio:SIO_000628
miriam-gene:1121
,
lld:C0678213
;
a
sio:SIO_001121
.
}
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_provenance
{
dgn-np:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_assertion
dcterms:description
"[To assess the relative accuracy of p57(KIP2) immunostaining and molecular diagnosis by nuclear DNA microsatellite polymorphisms in discriminating CHM from its mimics, we analyzed archival tissue from 33 case patients (7 with a definitive diagnosis of CHM, 16 with a possible diagnosis of HM, and 10 with normal placentas) by both methods.]. 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:16949913
;
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:NP374228.RA_9vKdyjCRwy96tmiN9_Dq5wah5ga7ls735MiHlo6WPQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}