@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_head
{
this:
np:hasAssertion
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_assertion
;
np:hasProvenance
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_provenance
;
np:hasPublicationInfo
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_assertion
a
np:Assertion
.
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_provenance
a
np:Provenance
.
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_assertion
{
miriam-gene:174
a
ncit:C16612
.
lld:C0152096
a
ncit:C7057
.
dgn-gda:DGN018d2cfcd31296b3a2984bcc5114cdd6
sio:SIO_000628
miriam-gene:174
,
lld:C0152096
;
a
sio:SIO_001121
.
}
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_provenance
{
dgn-np:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_assertion
dcterms:description
"[The association of increased levels of AFP in cases of trisomy 18 with ventral wall defects and the slight increase in AFP in cases of sex chromosomal anomalies other than Turner's syndrome was found.]. 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:10951473
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP227810.RAvZjMrVga7ABDtVko73hHyAhxZFsMm09j5JMU-i1nE88130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:49+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}