@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M
> .
@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:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_head
{
this:
np:hasAssertion
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_assertion
;
np:hasProvenance
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_provenance
;
np:hasPublicationInfo
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_assertion
a
np:Assertion
.
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_provenance
a
np:Provenance
.
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_assertion
{
miriam-gene:10167
a
ncit:C16612
.
lld:C2939175
a
ncit:C7057
.
dgn-gda:DGNd52e67fa75c437366acf7234e413caae
sio:SIO_000628
miriam-gene:10167
,
lld:C2939175
;
a
sio:SIO_001121
.
}
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_provenance
{
dgn-np:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_assertion
dcterms:description
"[Evaluation of the possible implication of ATB(0) in the intestinal phenotype of CF was performed on the basis of the functional characteristics of the encoded protein, its apparent relevance to meconium ileus (MI) and position in relation to the hCFM1 syntenic region.]. 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:11781704
;
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:NP215002.RAH7398Nr2bpxrg_EiwF-WpxZs45HjenNvf9fpRPsOA8M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}