@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms
> .
@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:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_head
{
this:
np:hasAssertion
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_assertion
;
np:hasProvenance
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_provenance
;
np:hasPublicationInfo
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_assertion
a
np:Assertion
.
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_provenance
a
np:Provenance
.
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_assertion
{
miriam-gene:3939
a
ncit:C16612
.
lld:C0001916
a
ncit:C7057
.
dgn-gda:DGNce3d446d988aa00b8567d10b97e40580
sio:SIO_000628
miriam-gene:3939
,
lld:C0001916
;
a
sio:SIO_001121
.
}
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_provenance
{
dgn-np:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_assertion
dcterms:description
"[Since HBB is syntenic with catalase (CAT) in both humans and cattle, while catalase is asyntenic with HBB in mice, at least two chromosomal rearrangements are required to account for the chromosomal relationships of HBB, CAT, LDHA, and the albino locus in these three species.]. 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:7930500
;
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:NP651362.RAngRrZL2_whaGA9GzQ1wx6rfCHxSLeS1pZGMPXH9D_Ms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}