Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_assertion description "[Scapuloperoneal spinal muscular atrophy (SPSMA) and hereditary motor and sensory neuropathy type IIC (HMSN IIC, also known as HMSN2C or Charcot-Marie-Tooth disease type 2C (CMT2C)) are phenotypically heterogeneous disorders involving topographically distinct nerves and muscles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_assertion evidence source_evidence_literature NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_assertion SIO_000772 20037587 NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_assertion wasDerivedFrom befree-20140225 NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_assertion wasGeneratedBy ECO_0000203 NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447869.RAU0c4pmsvH5zblemi9SnNK6DzeaBJW0FzW_2BTIXGuio130_provenance.