@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw
> .
@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:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_head
{
this:
np:hasAssertion
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_assertion
;
np:hasProvenance
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_provenance
;
np:hasPublicationInfo
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_assertion
a
np:Assertion
.
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_provenance
a
np:Provenance
.
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_assertion
{
miriam-gene:5555
a
ncit:C16612
.
lld:C0745103
a
ncit:C7057
.
dgn-gda:DGNb7e3c22f551bee3c77d1d7c8a89f056f
sio:SIO_000628
miriam-gene:5555
,
lld:C0745103
;
a
sio:SIO_001121
.
}
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_provenance
{
dgn-np:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_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:NP203788.RAVBBnDC1e1ihzHk2RIPx135g3egr42g2pXQcrt6Jo2bw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}