@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic
> .
@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:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_head
{
this:
np:hasAssertion
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion
;
np:hasProvenance
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance
;
np:hasPublicationInfo
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion
a
np:Assertion
.
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance
a
np:Provenance
.
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C0011436
a
ncit:C7057
.
dgn-gda:DGN8638bd225d3bdc5696a4204d7e53b5e2
sio:SIO_000628
miriam-gene:6696
,
lld:C0011436
;
a
sio:SIO_001121
.
}
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_provenance
{
dgn-np:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_assertion
dcterms:description
"[Dentinogenesis imperfecta type II and dentin dysplasia type II are diseases resulting in abnormal dentin formation, which have been mapped to overlapping regions of human chromosome 4q defined by markers D4S2691 and D4S2692 (6.6 cM) and D4S3291 and SPP1 (14.1 cM), respectively.]. 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:9541230
;
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:NP854263.RAkiPpwKW8mfZ3LBlsGjED4wnLU1s_BphkwQNeO_Y75ic130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}