Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_assertion description "[Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_assertion evidence source_evidence_curated NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_assertion SIO_000772 10802654 NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_assertion wasDerivedFrom uniprot-2016 NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_assertion wasGeneratedBy ECO_0000218 NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP800.RA_VKm8AeKZ_tH-ffLo6CxGAB8DPZ8bMxv0gNv4cfh9Vg130_provenance.