@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI
> .
@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:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_head
{
this:
np:hasAssertion
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion
;
np:hasProvenance
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance
;
np:hasPublicationInfo
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion
a
np:Assertion
.
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance
a
np:Provenance
.
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion
{
miriam-gene:147495
a
ncit:C16612
.
lld:C0023195
a
ncit:C7057
.
dgn-gda:DGN392944e99ef85786c4c4a9708dec1917
sio:SIO_000628
miriam-gene:147495
,
lld:C0023195
;
a
sio:SIO_001121
.
}
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_provenance
{
dgn-np:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_assertion
dcterms:description
"[These included membrane cholesterol content (increased in homozygotes with LCAT deficiency), changes in sodium and potassium content and Na+,k+-ATPase activity (the latter being increased in HHS), changes in acetylcholinesterase and sulfhydryl group latency (present in LCAT deficiency, but not in HHS) and 2,3 DPG content (decreased in HHS, normal in LCAT deficiency.]. 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:6246569
;
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:NP246055.RAiFuZoo3hhG7knp9FdFBivoaQc3HFlfVayD7ACI2ttWI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}