Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion> ?p ?o ?g. }
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- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion type Assertion NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_head.
- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion description "[Studies further define the molecular heterogeneity of the alpha-Gal A mutations in classical Fabry disease, permit precise heterozygote detection and prenatal diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_provenance.
- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion evidence source_evidence_literature NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_provenance.
- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion SIO_000772 16595074 NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_provenance.
- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion wasDerivedFrom lhgdn-20090331 NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_provenance.
- NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_assertion wasGeneratedBy ECO_0000203 NP150466.RAmpG7NxcEqvcqWZpoidvYltP7Ix9XlXbmI-pVEVfSre8130_provenance.