Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_assertion description "[Clinical variability of Waardenburg-Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_assertion evidence source_evidence_literature NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_assertion SIO_000772 19764031 NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_assertion wasDerivedFrom befree-2016 NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_assertion wasGeneratedBy ECO_0000203 NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.
- befree-2016 importedOn "2016-02-19" NP764163.RAaqSllv4qe4tIvqc0b3wPiE6VsxHRa1t2DZmn4Ei23KA130_provenance.