@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8
> .
@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:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_head
{
this:
np:hasAssertion
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_assertion
;
np:hasProvenance
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_provenance
;
np:hasPublicationInfo
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_assertion
a
np:Assertion
.
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_provenance
a
np:Provenance
.
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGNa47f268ec4a7e4e20f226ffc281f1b1e
sio:SIO_000628
miriam-gene:7276
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_provenance
{
dgn-np:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_assertion
dcterms:description
"[Finally, from the viewpoint of molecular evolution of TTR in primates, we determined that human TTR mutations causing the leptomeningeal phenotype of TTR amyloidosis tended to occur in amino acid residues that showed no diversity throughout primate evolution.]. 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:22184092
;
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:NP947980.RAPk78-RANu8BySpm9XJHvO7fJUiIlStgmNIRUZsg_vm8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:54+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" .
}