@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI
> .
@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:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_head
{
this:
np:hasAssertion
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_assertion
;
np:hasProvenance
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_assertion
a
np:Assertion
.
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_provenance
a
np:Provenance
.
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_assertion
{
miriam-gene:537
a
ncit:C16612
.
lld:C1861355
a
ncit:C7057
.
dgn-gda:DGN9f9f495205407d1b5a802354bd24a80d
sio:SIO_000628
miriam-gene:537
,
lld:C1861355
;
a
sio:SIO_001121
.
}
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_provenance
{
dgn-np:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_assertion
dcterms:description
"[Another clone (SD2), however, has the potential to encode two proteins: a 170 amino acids polypeptide starting at the optimal first ATG has no detectable homology with any other proteins currently in the data bases, and another ORF beginning at the suboptimal second startcodon which is identical to that of SD4.]. 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:1454518
;
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:NP279936.RANSnyQArTewN6PiIA8nyJ7kKRaT9qR_mDNqKlKcdSOOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}