@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA
> .
@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:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_head
{
this:
np:hasAssertion
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_assertion
;
np:hasProvenance
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_assertion
a
np:Assertion
.
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_provenance
a
np:Provenance
.
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_assertion
{
miriam-gene:5555
a
ncit:C16612
.
lld:C0949658
a
ncit:C7057
.
dgn-gda:DGN81dff64c9015e8fbad979c44b9eb8181
sio:SIO_000628
miriam-gene:5555
,
lld:C0949658
;
a
sio:SIO_001121
.
}
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_provenance
{
dgn-np:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_assertion
dcterms:description
"[Mutations in MyBPC are strongly associated with the heart disease familial hypertrophic cardiomyopathy (FHC) and these experiments of nature have provided some insight into the intricate workings of this protein in the heart.]. 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:15115610
;
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:NP505939.RA2ilA6OC5zBHxPfgo88NwvzgJ_7EZRpnwiowWuQdySxA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}