@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE
> .
@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:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_head
{
this:
np:hasAssertion
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_assertion
;
np:hasProvenance
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_assertion
a
np:Assertion
.
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_provenance
a
np:Provenance
.
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_assertion
{
miriam-gene:56928
a
ncit:C16612
.
lld:C0276496
a
ncit:C7057
.
dgn-gda:DGN760cf1e5dee92bd2686095674146fd94
sio:SIO_000628
miriam-gene:56928
,
lld:C0276496
;
a
sio:SIO_001121
.
}
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_provenance
{
dgn-np:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_assertion
dcterms:description
"[We have introduced the FAD-associated PS1 G384A mutation, which occurs within the highly conserved GXGD motif of PS1 right next to the catalytically critical aspartate residue, into the corresponding GXGD motif of the signal peptide peptidase-like 2b (SPPL2b).]. 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:18768471
;
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:NP238496.RA1xxdL7zMUhbti_uaohcG0Hc8x4Gc31C4iKG3GemKlWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}