Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- befree-2016 importedOn "2016-02-19" NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_assertion wasGeneratedBy ECO_0000203 NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_assertion wasDerivedFrom befree-2016 NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_assertion SIO_000772 17236141 NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_assertion evidence source_evidence_literature NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.
- NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_assertion description "[Our data established the link between HOXD13 and two additional limb phenotypes--syndactyly type V and brachydactyly type A4--and demonstrated that a polyalanine contraction in HOXD13, most likely, led to other digital anomalies but not to synpolydactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589658.RAwKYUaHfT5Wk8Kivmo3cNZMwRzlSD72p2wUxqXhf9jU8130_provenance.