@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI
> .
@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:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_head
{
this:
np:hasAssertion
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_assertion
;
np:hasProvenance
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_provenance
;
np:hasPublicationInfo
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_assertion
a
np:Assertion
.
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_provenance
a
np:Provenance
.
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_assertion
{
miriam-gene:1028
a
ncit:C16612
.
lld:C0020217
a
ncit:C7057
.
dgn-gda:DGN92e5076e74b78c4829c4315440d8c98f
sio:SIO_000628
miriam-gene:1028
,
lld:C0020217
;
a
sio:SIO_001121
.
}
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_provenance
{
dgn-np:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_assertion
dcterms:description
"[Recent studies have demonstrated the value of ancillary techniques, including p57 immunohistochemistry and short tandem repeat genotyping, for distinguishing hydatidiform moles (HM) from nonmolar specimens and for subtyping HMs as complete hydatidiform moles (CHM) and partial hydatidiform moles (PHM).]. 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:23370656
;
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:NP204209.RAYxKErsrQNxl2d0o9x5mTbjGF3pXOv0bNNMXjHEYVbfI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}