@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA
> .
@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:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_head
{
this:
np:hasAssertion
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_assertion
;
np:hasProvenance
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_provenance
;
np:hasPublicationInfo
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_assertion
a
np:Assertion
.
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_provenance
a
np:Provenance
.
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_assertion
{
miriam-gene:94081
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN2d2ad1c953075dbd41cfbfeaf2dffa90
sio:SIO_000628
miriam-gene:94081
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_provenance
{
dgn-np:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_assertion
dcterms:description
"[The absence of the disease-associated paternal alleles in TCC samples from two pregnancies at risk for spinal muscular atrophy and myotonic dystrophy predicted unaffected fetuses in agreement with subsequent results on chorionic villi and newborns' leukocytes.]. 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:8566945
;
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:NP183422.RAne3BdtOspW17KXNLc_biNFTzklI7QvNIqvL852UHGiA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}