@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_head
{
this:
np:hasAssertion
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_assertion
;
np:hasProvenance
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_assertion
a
np:Assertion
.
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_provenance
a
np:Provenance
.
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_assertion
{
miriam-gene:3931
a
ncit:C16612
.
lld:C0023195
a
ncit:C7057
.
dgn-gda:DGNc2371b18b04f86b6c10ab044e8c55fdb
sio:SIO_000628
miriam-gene:3931
,
lld:C0023195
;
a
sio:SIO_001121
.
}
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_provenance
{
dgn-np:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_assertion
dcterms:description
"[More recent studies in human LCAT gene mutation carriers tend to suggest that atherogenicity in LCAT deficiency may be dependent on the nature of the mutations, providing plausible explanations for the otherwise contradictory findings.]. 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:22326749
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP960216.RAB3HDs43R95ppQzGbUe8pDZv_hVvqz6-hlr2vX3JIFAw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}