Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_assertion description "[Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_assertion evidence source_evidence_literature NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_assertion SIO_000772 19293842 NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_assertion wasDerivedFrom befree-20150227 NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_assertion wasGeneratedBy ECO_0000203 NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568270.RAfVKuX957CHhQ4X6IIbs1PX29-UmLC2ay-vRx5iMp0ZA130_provenance.