@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss
> .
@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:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_head
{
this:
np:hasAssertion
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_assertion
;
np:hasProvenance
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_provenance
;
np:hasPublicationInfo
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_assertion
a
np:Assertion
.
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_provenance
a
np:Provenance
.
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGN313de068f3ac7560f2b9736c0c28badc
sio:SIO_000628
miriam-gene:5660
,
lld:C0263214
;
a
sio:SIO_001121
.
}
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_provenance
{
dgn-np:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_assertion
dcterms:description
"[In contrast, Arg169Trp and Val297Met substitutions, both occurring at CG dinucleotides, were commonly observed in not only Japanese but also Western populations, indicating that these are hot spots for mutation in the protein C gene.]. 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:8883262
;
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:NP768476.RAaVc3AcOA9cETkG9PgqwN94dm7ORfksS1CIWBhzLNgss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}