Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion type Assertion NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_head.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion evidence source_evidence_literature NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion SIO_000772 11030761 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion wasDerivedFrom befree-2016 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion wasGeneratedBy ECO_0000203 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.