@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw
> .
@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:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_head
{
this:
np:hasAssertion
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_assertion
;
np:hasProvenance
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_provenance
;
np:hasPublicationInfo
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_assertion
a
np:Assertion
.
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_provenance
a
np:Provenance
.
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_assertion
{
miriam-gene:6360
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGN5dcaf17c472a7ebcf4d66bf943dd1f69
sio:SIO_000628
miriam-gene:6360
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_provenance
{
dgn-np:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_assertion
dcterms:description
"[While analyzing the melatonin synthetic pathways of Long Evans cinnamon (LEC) rats mutant for PINA, a pineal night-specific ATPase defective in Wilson disease, we discovered that NAT activity and protein levels are greatly reduced in LEC rats, and that the highly conserved histidine 28 is mutated to tyrosine.]. 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:15978062
;
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:NP697929.RAXMQaiG5oxSYfcbpisdIuL50qqjKoE887SW-tE9tr0vw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}