@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso
> .
@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:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_head
{
this:
np:hasAssertion
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_assertion
;
np:hasProvenance
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_provenance
;
np:hasPublicationInfo
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_assertion
a
np:Assertion
.
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_provenance
a
np:Provenance
.
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_assertion
{
miriam-gene:5555
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGNe3ea50490520931926d95b1e91b0290c
sio:SIO_000628
miriam-gene:5555
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_provenance
{
dgn-np:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_assertion
dcterms:description
"[While mutations in different myosin binding protein C (MYBPC) genes are well known causes of various human diseases, such as hypertrophic (HCM) and dilated (DCM) forms of cardiomyopathy as well as skeletal muscular disorders, the underlying molecular mechanisms remain not well understood.]. 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:22173300
;
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:NP708699.RAPDkPh3y5W_CStV27GEmjGwkgMYWQuI_jlvNydIdVBso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}