@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_head
{
this:
np:hasAssertion
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion
;
np:hasProvenance
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance
;
np:hasPublicationInfo
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion
a
np:Assertion
.
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance
a
np:Provenance
.
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion
{
miriam-gene:1287
a
ncit:C16612
.
lld:C0241908
a
ncit:C7057
.
dgn-gda:DGNb8785cb45ae9e9ab5e610318af0fd6fc
sio:SIO_000628
miriam-gene:1287
,
lld:C0241908
;
a
sio:SIO_001121
.
}
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance
{
dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion
dcterms:description
"[This result suggests that COL4A5 should be added to the list of causative genes for benign familial hematuria, although the mechanism(s) by which the same mutation leads to the distinct phenotypes, i.e.]. 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:19937058
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:37+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}