Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion evidence source_evidence_curated NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion SIO_000772 20817137 NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion wasDerivedFrom uniprot-2016 NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion wasGeneratedBy ECO_0000218 NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.