@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8
> .
@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:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_head
{
this:
np:hasAssertion
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_assertion
;
np:hasProvenance
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_provenance
;
np:hasPublicationInfo
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_assertion
a
np:Assertion
.
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_provenance
a
np:Provenance
.
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_assertion
{
miriam-gene:10518
a
ncit:C16612
.
lld:C0678213
a
ncit:C7057
.
dgn-gda:DGN54a46208b1e5004dc06a5041d8416371
sio:SIO_000628
miriam-gene:10518
,
lld:C0678213
;
a
sio:SIO_001121
.
}
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_provenance
{
dgn-np:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_assertion
dcterms:description
"[Pathological review and genotyping of other molar pregnancies in these cases showed them to be typical CHM with negative p57(KIP2) immunostaining of the cytotrophoblast cells and villous stroma and to be diploid but biparental, confirming a diagnosis of familial recurrent hydatidiform mole (FRHM).]. 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:23125094
;
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:NP232928.RAIAxm0v8Tveynr7DeAyt4zvZQ7cPhd66B0VJ3LbcS2P8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}