Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion> ?p ?o ?g. }
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- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion type Assertion NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_head.
- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.
- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion evidence source_evidence_literature NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.
- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion SIO_000772 12840783 NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.
- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion wasDerivedFrom befree-20150227 NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.
- NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion wasGeneratedBy ECO_0000203 NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.