@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY
> .
@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:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_head
{
this:
np:hasAssertion
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_assertion
;
np:hasProvenance
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_provenance
;
np:hasPublicationInfo
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_assertion
a
np:Assertion
.
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_provenance
a
np:Provenance
.
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_assertion
{
miriam-gene:7504
a
ncit:C16612
.
lld:C0687751
a
ncit:C7057
.
dgn-gda:DGNe292255860c0e9da969da8312e6ca660
sio:SIO_000628
miriam-gene:7504
,
lld:C0687751
;
a
sio:SIO_001121
.
}
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_provenance
{
dgn-np:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_assertion
dcterms:description
"[The McLeod phenotype is derived from various forms of XK gene defects that result in the absence of XK protein, and is defined hematologically by the absence of Kx antigen, weakening of Kell system antigens, and red cell acanthocytosis.]. 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:17300882
;
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:NP669099.RAdtxEhP5KlSgStypWIyQgVVRXmIm2BOruLXrwVsb9LmY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}