Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion> ?p ?o ?g. }
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- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion type Assertion NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_head.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion evidence source_evidence_literature NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion SIO_000772 19247433 NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion wasDerivedFrom befree-2016 NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion wasGeneratedBy ECO_0000203 NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.