Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion type Assertion NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_head.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion description "[Compound heterozygous mutations of the TNXB gene cause primary myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_provenance.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion evidence source_evidence_literature NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_provenance.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion SIO_000772 23768946 NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_provenance.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion wasDerivedFrom befree-20150227 NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_provenance.
- NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_assertion wasGeneratedBy ECO_0000203 NP748882.RAUN1eLpiOMohIbAOfVlgJ0jYDymiJwBUypDyTtfwSxR8130_provenance.