@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU
> .
@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:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_head
{
this:
np:hasAssertion
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_assertion
;
np:hasProvenance
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_assertion
a
np:Assertion
.
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_provenance
a
np:Provenance
.
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_assertion
{
miriam-gene:11151
a
ncit:C16612
.
lld:C0678213
a
ncit:C7057
.
dgn-gda:DGN5c98e4fb3a73ebfd2953e8adcda42778
sio:SIO_000628
miriam-gene:11151
,
lld:C0678213
;
a
sio:SIO_001121
.
}
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_provenance
{
dgn-np:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_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:NP744635.RAWjrLQQH90zKuNDuQMI8xNXlJcHIXRRFz69uFb3pFTUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}