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- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion type Assertion NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_head.
- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion description "[Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_provenance.
- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion evidence source_evidence_literature NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_provenance.
- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion SIO_000772 24015686 NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_provenance.
- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion wasDerivedFrom befree-20150227 NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_provenance.
- NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_assertion wasGeneratedBy ECO_0000203 NP947832.RAEVdiJ271MQGLW1F9x9oC1D4Yfk9r6zEEWAjbszg7uO4130_provenance.