@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0
> .
@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/v3.0.0/void/
> .
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_head
{
this:
np:hasAssertion
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion
;
np:hasProvenance
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance
;
np:hasPublicationInfo
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion
a
np:Assertion
.
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance
a
np:Provenance
.
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0949658
a
ncit:C7057
.
dgn-gda:DGNc77e0338b3562d307d0fbf0d1cb687be
sio:SIO_000628
miriam-gene:3133
,
lld:C0949658
;
a
sio:SIO_001121
.
}
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_provenance
{
dgn-np:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_assertion
dcterms:description
"[While missense mutations in the beta cardiac myosin heavy chain (MHC) gene account for approximately half of all cases of familial hypertrophic cardiomyopathy, the molecular causes of sporadic hypertrophic cardiomyopathy are unknown.]. 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:1430197
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP458518.RA9E84i6pQ_3kfDDpvAGbKGa3uHBwnedqFnLxv7mIerj0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:09+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}