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- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion type Assertion NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_head.
- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion wasGeneratedBy ECO_0000203 NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_provenance.
- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion wasDerivedFrom befree-2016 NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_provenance.
- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion SIO_000772 20375002 NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_provenance.
- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion evidence source_evidence_literature NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_provenance.
- NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_assertion description "[on mutations in the fibrillin-1 gene in patients with skin fibrosis (stiff skin) adds a new piece of information on a connective tissue disorder that resembles systemic sclerosis, an autoimmune disease characterized by skin fibrosis and visceral organ involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804774.RA1_jEQoXYARDPdjDbGDunQa0egDHc4tNfaV0tCgauwgE130_provenance.