@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w
> .
@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:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_head
{
this:
np:hasAssertion
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion
;
np:hasProvenance
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion
a
np:Assertion
.
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance
a
np:Provenance
.
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion
{
miriam-gene:7299
a
ncit:C16612
.
lld:C0019880
a
ncit:C7057
.
dgn-gda:DGN537a0e40496fbfcac26e124f7e54e398
sio:SIO_000628
miriam-gene:7299
,
lld:C0019880
;
a
sio:SIO_001121
.
}
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance
{
dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion
dcterms:description
"[Our data suggest that reversible hypopigmentation in homocystinuria is the result of tyrosinase inhibition by homocyst(e)ine and that the probable mechanism of this inhibition is the interaction of homocyst(e)ine with copper at the active site of tyrosinase.]. 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:7611281
;
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:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}