@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc
> .
@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:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_head
{
this:
np:hasAssertion
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_assertion
;
np:hasProvenance
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_assertion
a
np:Assertion
.
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_provenance
a
np:Provenance
.
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_assertion
{
miriam-gene:2584
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGN24a5b09da8b18b6dfd461c2babb86d2c
sio:SIO_000628
miriam-gene:2584
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_provenance
{
dgn-np:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_assertion
dcterms:description
"[In man, defects in galactose metabolism can result in disorders with severe clinical consequences, and deficiencies in galactokinase have been linked with the development of cataracts within the first few months of life.]. 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:15003454
;
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:NP620995.RAuxH_Qrj9VZI2d8Gv9ios_Tafk-dakKj6iQTFxiiwOBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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" .
}