@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg
> .
@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:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_head
{
this:
np:hasAssertion
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_assertion
;
np:hasProvenance
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_assertion
a
np:Assertion
.
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_provenance
a
np:Provenance
.
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_assertion
{
miriam-gene:728358
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN38e345ed11a79b5801aef107e9aa2dba
sio:SIO_000628
miriam-gene:728358
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_provenance
{
dgn-np:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_assertion
dcterms:description
"[Among the malaria patients, the Hp1-1 phenotype was significantly more prevalent among patients with the complications of cerebral malaria and severe anaemia compared to patients with uncomplicated disease, whereas the reverse was seen with respect to Hp2-1 and Hp2-2.]. 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:10897372
;
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:NP930244.RAREVEuTwN0eOcKEwx4R0WP0VnQO0s4TlsQzcJYAdjRAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}