@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g
> .
@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:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_head
{
this:
np:hasAssertion
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_assertion
;
np:hasProvenance
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_assertion
a
np:Assertion
.
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_provenance
a
np:Provenance
.
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_assertion
{
miriam-gene:11151
a
ncit:C16612
.
lld:C0027960
a
ncit:C7057
.
dgn-gda:DGNc69983d339bdb12351e499321eccd7c5
sio:SIO_000628
miriam-gene:11151
,
lld:C0027960
;
a
sio:SIO_001121
.
}
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_provenance
{
dgn-np:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_assertion
dcterms:description
"[In all cases, the pathologic diagnoses were easily resolved: two cases were partial moles (triploid, p57 positive), two cases were early complete moles (diploid, p57 negative), and two cases were twin gestations with normal villi (diploid, p57 positive) admixed with villi from a complete hydatidiform mole (diploid, p57 negative).]. 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:12063872
;
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:NP378967.RAXvvV9cWLmzMS4V5S59HqCrFCfczhHG01TcJKZeiKA6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}