@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE
> .
@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:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_head
{
this:
np:hasAssertion
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_assertion
;
np:hasProvenance
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_provenance
;
np:hasPublicationInfo
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_assertion
a
np:Assertion
.
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_provenance
a
np:Provenance
.
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_assertion
{
miriam-gene:10058
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNb7f3ac0237873de40f764839bcbc1c44
sio:SIO_000628
miriam-gene:10058
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_provenance
{
dgn-np:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_assertion
dcterms:description
"[ABC genes are essential for many processes in the cell, and mutations in these genes cause or contribute to several human genetic disorders including cystic fibrosis, neurological disease, retinal degeneration, cholesterol and bile transport defects, anemia, and drug response.]. 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:11441126
;
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:NP672801.RAJx2alhMXSWz-1TxvzMgEjZAUefT-MnvNOsavnuTOIqE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}