Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion> ?p ?o ?g. }
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- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion type Assertion NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_head.
- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_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." NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_provenance.
- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion evidence source_evidence_literature NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_provenance.
- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion SIO_000772 20037587 NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_provenance.
- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion wasDerivedFrom befree-20150227 NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_provenance.
- NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_assertion wasGeneratedBy ECO_0000203 NP935184.RAh21PG_Sx1rkZ8Zairki1KYlA1cx4AykbaZ-DkEkB1GU130_provenance.