@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0
> .
@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:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_head
{
this:
np:hasAssertion
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_assertion
;
np:hasProvenance
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_assertion
a
np:Assertion
.
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_provenance
a
np:Provenance
.
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_assertion
{
miriam-gene:11151
a
ncit:C16612
.
lld:C0333693
a
ncit:C7057
.
dgn-gda:DGNfb55593c3349d6bc4269c7aaab5ec0e6
sio:SIO_000628
miriam-gene:11151
,
lld:C0333693
;
a
sio:SIO_001121
.
}
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_provenance
{
dgn-np:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_assertion
dcterms:description
"[Immunohistochemical assessment of the paternally imprinted, maternally expressed p57 gene can identify CHMs (androgenetic diploidy) by their lack of p57 expression, but cannot distinguish PHMs (diandric monogynic triploidy) from NMs (biparental diploidy).]. 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:19815697
;
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:NP783617.RA8Jm_Ck1UBXHaNoftN-VtDm1DS4Blko8hvXl9lxkteQ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}