@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco
> .
@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:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_head
{
this:
np:hasAssertion
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_assertion
;
np:hasProvenance
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_provenance
;
np:hasPublicationInfo
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_assertion
a
np:Assertion
.
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_provenance
a
np:Provenance
.
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_assertion
{
miriam-gene:6007
a
ncit:C16612
.
lld:C0014761
a
ncit:C7057
.
dgn-gda:DGN17a4c3fe361e2df2827ef7d6ef40b111
sio:SIO_000628
miriam-gene:6007
,
lld:C0014761
;
a
sio:SIO_001122
.
}
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_provenance
{
dgn-np:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_assertion
dcterms:description
"[ In a limited screen at the molecular level among 1000 random D+ donors in southwestern Germany, 20 donors were found carrying aberrant RHD alleles. Four of these alleles were new and likely sporadic. An estimate was derived of the variety that may be enc]. 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:15987365
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80187.RA0HXxlXgC66tZRuv5KKRnSp7pXr42U9NMZcVq2HNyVco130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:24+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" .
}