@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes
> .
@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:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_head
{
this:
np:hasAssertion
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_assertion
;
np:hasProvenance
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_provenance
;
np:hasPublicationInfo
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_assertion
a
np:Assertion
.
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_provenance
a
np:Provenance
.
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN7b5a076bb177d321a80ed26223e301a9
sio:SIO_000628
miriam-gene:1080
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_provenance
{
dgn-np:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_assertion
dcterms:description
"[In some cases, CFTR mutations have been identified in adults presenting with isolated features of cystic fibrosis such as mild lung disease, pancreatic insufficiency or male infertility, with normal sweat duct function.]. 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:9466061
;
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:NP449997.RABvWyuztdjkQhwo7i1oDYc6pI8Pq0oKYIDQ2gAyJyzes130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}