@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY
> .
@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:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_head
{
this:
np:hasAssertion
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_assertion
;
np:hasProvenance
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_provenance
;
np:hasPublicationInfo
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_assertion
a
np:Assertion
.
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_provenance
a
np:Provenance
.
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_assertion
{
miriam-gene:7021
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN4e8b44e439e5b283356696e616a57374
sio:SIO_000628
miriam-gene:7021
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_provenance
{
dgn-np:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_assertion
dcterms:description
"[The analysis did not show any of the five mutations of TFAP2B screened by massARRAY in patients and controls, indicating that these mutations were not involved in the manifestation of CHD in the patients at Mysore, south India.]. 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:22199100
;
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:NP360760.RAX0ee65kmxPNJhEz7oc1TllRxOH29Chv3NnkCrzCFhlY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}