@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA
> .
@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:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_head
{
this:
np:hasAssertion
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_assertion
;
np:hasProvenance
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_assertion
a
np:Assertion
.
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_provenance
a
np:Provenance
.
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_assertion
{
miriam-gene:3892
a
ncit:C16612
.
lld:C0221260
a
ncit:C7057
.
dgn-gda:DGNe9d6e24a9f1134fc44ec413d71b1cdbe
sio:SIO_000628
miriam-gene:3892
,
lld:C0221260
;
a
sio:SIO_001121
.
}
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_provenance
{
dgn-np:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_assertion
dcterms:description
"[A comparison of clinical features and severity between cases with hHb1 and hHb6 mutations does not suggest distinct effects on phenotype, with the possible exception of nail dystrophy, commoner with hHb1 defects.]. 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:10504448
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP529819.RA4rMvJ0RzHlF-wFYBd5xNgsxKEWYgps_6pvCq3anYCUA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:53+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" .
}