@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw
> .
@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:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_head
{
this:
np:hasAssertion
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion
;
np:hasProvenance
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance
;
np:hasPublicationInfo
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion
a
np:Assertion
.
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance
a
np:Provenance
.
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion
{
miriam-gene:258
a
ncit:C16612
.
lld:C0002452
a
ncit:C7057
.
dgn-gda:DGNf9ffa8c645cc06ade8719209b0dc87f5
sio:SIO_000628
miriam-gene:258
,
lld:C0002452
;
a
sio:SIO_001121
.
}
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_provenance
{
dgn-np:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_assertion
dcterms:description
"[An identified human enamelin BAC genomic clone was shown to contain markers D4S2604 and D4S2670, as well as the first exon of the human ameloblastin gene, placing enamelin in the critical amelogenesis imperfecta locus between markers HIS1 and D4S2604 at 4q21.]. 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:11037750
;
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:NP796884.RAKyothJSmLn2i3SnNVsiQF_7_xf9LH5o_lvka35IM2Gw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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: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" .
}