@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g
> .
@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:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_head
{
this:
np:hasAssertion
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_assertion
;
np:hasProvenance
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_assertion
a
np:Assertion
.
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_provenance
a
np:Provenance
.
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_assertion
{
miriam-gene:961
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGN555458f543484fdd1c689ec7973aa840
sio:SIO_000628
miriam-gene:961
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_provenance
{
dgn-np:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_assertion
dcterms:description
"[Since these cells are morphologically normal with no sign of hemolysis, it is assumed that CD47 deficiency per se is not responsible for the cell shape abnormalities and for the compensated hemolytic anemia typical of 4.2(-) and Rh(null) red cells.]. 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:12393467
;
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:NP922609.RAaicvvNu9DbZPO_HOWFkB-iKRUnpZWb_WU36fSSv1C-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}