Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_assertion description "[BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dub� syndrome: a new series of 50 families and a review of published reports.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_assertion evidence source_evidence_literature NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_assertion SIO_000772 18234728 NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_assertion wasDerivedFrom befree-2016 NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_assertion wasGeneratedBy ECO_0000203 NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.
- befree-2016 importedOn "2016-02-19" NP652675.RAhRqvFkK9iWQ4Z0KclUWs8A9jJEk47He4IOuoRHeBCic130_provenance.