@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik
> .
@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:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_head
{
this:
np:hasAssertion
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_assertion
;
np:hasProvenance
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_provenance
;
np:hasPublicationInfo
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_assertion
a
np:Assertion
.
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_provenance
a
np:Provenance
.
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_assertion
{
miriam-gene:4634
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGN04de0b232896fb05e2b23cde40b31d1a
sio:SIO_000628
miriam-gene:4634
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_provenance
{
dgn-np:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_assertion
dcterms:description
"[We analysed 186 unrelated individuals with HCM for the human ventricular myosin regulatory (MYL2) and essential light chain genes (MYL3) using polymerase chain reaction, single strand conformation polymorphism analysis and automated sequencing.]. 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:12404107
;
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:NP378264.RAHTZWoXU94BiIP7VMPfilkMjK4x_ExDmMhQpfo0YAWik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}