@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA
> .
@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:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_head
{
this:
np:hasAssertion
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_assertion
;
np:hasProvenance
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_assertion
a
np:Assertion
.
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_provenance
a
np:Provenance
.
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0152096
a
ncit:C7057
.
dgn-gda:DGNb2d14eacfcd956cd1adbb5cbfecc7c1f
sio:SIO_000628
miriam-gene:3342
,
lld:C0152096
;
a
sio:SIO_001121
.
}
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_provenance
{
dgn-np:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_assertion
dcterms:description
"[These findings suggest that in trisomy 18 the decrease in maternal serum concentration of HCG subunits results from an impairment in the transcription of the corresponding gene which affects the beta subunit to a greater extent than the I subunit.]. 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:9238717
;
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:NP894827.RALtmO1Q1CnMWpW8tje6iZDldjUffThgVhOpEqENJ6MyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}