@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg
> .
@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:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_head
{
this:
np:hasAssertion
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_assertion
;
np:hasProvenance
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_assertion
a
np:Assertion
.
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_provenance
a
np:Provenance
.
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_assertion
{
miriam-gene:64061
a
ncit:C16612
.
lld:C0002876
a
ncit:C7057
.
dgn-gda:DGN5b091e7fda72b75fb6c093d6e1fe5928
sio:SIO_000628
miriam-gene:64061
,
lld:C0002876
;
a
sio:SIO_001121
.
}
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_provenance
{
dgn-np:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_assertion
dcterms:description
"[Neither deficiency of CD44 nor absence of Colton antigens are general features of CDA because erythrocytes from patients with CDA I, CDA II, CDA III, and two other unclassified CDAs had normal expression of CD44 and normal Colton blood group phenotypes.]. 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:7507739
;
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:NP594429.RABohvmggSA7vjowbmfjlTmBzNwkwj2COpJUHBf497FAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}