@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80
> .
@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:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_head
{
this:
np:hasAssertion
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_assertion
;
np:hasProvenance
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_provenance
;
np:hasPublicationInfo
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_assertion
a
np:Assertion
.
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_provenance
a
np:Provenance
.
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_assertion
{
miriam-gene:1028
a
ncit:C16612
.
lld:C0020217
a
ncit:C7057
.
dgn-gda:DGN41f62a0f85eb36ad0a567eb945eafb65
sio:SIO_000628
miriam-gene:1028
,
lld:C0020217
;
a
sio:SIO_001121
.
}
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_provenance
{
dgn-np:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_assertion
dcterms:description
"[The unique genetic features of CHMs (androgenetic diploidy), PHMs (diandric triploidy), and nonmolar specimens (biparental diploidy) allow for certain molecular techniques, including immunohistochemical analysis of p57 expression (a paternally imprinted maternally expressed gene) and molecular genotyping, to refine the diagnosis of hydatidiform moles.]. 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:21293291
;
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:NP430848.RAK6n_wV3v0STcvZK7pWcN7RVthA6csJopbYmlO2INx80130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}