Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_assertion description "[Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_assertion evidence source_evidence_literature NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_assertion SIO_000772 8664899 NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_assertion wasDerivedFrom befree-20150227 NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_assertion wasGeneratedBy ECO_0000203 NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568354.RAY3tkoHTCzkGq6VniGx5npwgy1FW9bf1L98v7jm0FCXc130_provenance.