Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion> ?p ?o ?g. }
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- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion type Assertion NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_head.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion evidence source_evidence_literature NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion SIO_000772 12632326 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion wasDerivedFrom befree-20140225 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion wasGeneratedBy ECO_0000203 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.