Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion> ?p ?o ?g. }
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- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion type Assertion NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_head.
- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion wasGeneratedBy ECO_0000203 NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_provenance.
- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion wasDerivedFrom befree-20140225 NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_provenance.
- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion SIO_000772 19615667 NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_provenance.
- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion evidence source_evidence_literature NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_provenance.
- NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_assertion description "[We found that recessive MAD is caused by homozygous loss of function of either MMP9 or MMP13, whereas dominant MAD is associated with missense mutations in the prodomain of MMP13 that determine autoactivation of MMP13 and intracellular degradation of both MMP13 and MMP9, resulting in a double enzymatic deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506198.RA0H8Ce90sF5N-yROSU_lwP09eK9W5S9KSoQkywCUuXzU130_provenance.