@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY
> .
@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:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_head
{
this:
np:hasAssertion
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_assertion
;
np:hasProvenance
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_assertion
a
np:Assertion
.
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_provenance
a
np:Provenance
.
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_assertion
{
miriam-gene:3931
a
ncit:C16612
.
lld:C0149676
a
ncit:C7057
.
dgn-gda:DGNc8f0ad909c066e64b0c8151735aece25
sio:SIO_000628
miriam-gene:3931
,
lld:C0149676
;
a
sio:SIO_001121
.
}
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_provenance
{
dgn-np:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_assertion
dcterms:description
"[It was found that both parents and one son had half the normal plasma LCAT activity whereas their only daughter and other son exhibited zero plasma LCAT activity, suggesting an autosomal co-dominant inheritance of the enzyme 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:7077125
;
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:NP932974.RAv3RNfLC-PCl8qwiXHvuAy21U0x9MBogSojwKqWxveMY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}