Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_assertion description "[Charcot-Marie-Tooth disease comprises a heterogeneous group of hereditary neuropathies which fall into two main groups: demyelinating CMT1 with reduced nerve conduction velocity and axonal CMT2 with normal nerve conduction velocity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_assertion evidence source_evidence_literature NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_assertion SIO_000772 14733962 NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_assertion wasDerivedFrom befree-2016 NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_assertion wasGeneratedBy ECO_0000203 NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.
- befree-2016 importedOn "2016-02-19" NP428719.RATvSXGy-nVBdOfb6eIAYq1cWPGck9nC0Jy8sknYWGHps130_provenance.