@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4
> .
@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:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_head
{
this:
np:hasAssertion
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_assertion
;
np:hasProvenance
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_provenance
;
np:hasPublicationInfo
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_assertion
a
np:Assertion
.
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_provenance
a
np:Provenance
.
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0745103
a
ncit:C7057
.
dgn-gda:DGNc2649a567a3dc0f94244d9c95a272f03
sio:SIO_000628
miriam-gene:6520
,
lld:C0745103
;
a
sio:SIO_001121
.
}
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_provenance
{
dgn-np:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_assertion
dcterms:description
"[Several mutations within the gene coding for the cardiac beta myosin heavy chain (designed MYH7) have been shown to be responsible for Familial Hypertrophic Cardiomyopathy (FHC) in several families, and evidence of genetic heterogeneity has been reported.]. 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:7815466
;
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:NP1322765.RA3wCVaXWzybf1gRnrYfFa6zv8F6Qt2967BTXWbMFRZz4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:46+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" .
}