Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion> ?p ?o ?g. }
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- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion type Assertion NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_head.
- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion description "[The authors' objective is to report two heterozygous missense mutations in the NDUFAF1 gene as a cause of fatal infantile HCM in a patient with isolated complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_provenance.
- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion evidence source_evidence_literature NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_provenance.
- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion SIO_000772 21931170 NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_provenance.
- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion wasDerivedFrom befree-20150227 NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_provenance.
- NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_assertion wasGeneratedBy ECO_0000203 NP901500.RAlCWNkxrYHmyhvDD9DoKVOXi0WR1iDFc_7r-znYHIcvc130_provenance.