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- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion type Assertion NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_head.
- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion description "[More recently mutations in the HESX1, the LHX3 and LHX4 transcription factor genes have also been described as a cause in patients with CPHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_provenance.
- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion evidence source_evidence_literature NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_provenance.
- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion SIO_000772 12812307 NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_provenance.
- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion wasDerivedFrom befree-20140225 NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_provenance.
- NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_assertion wasGeneratedBy ECO_0000203 NP536942.RAcSCgwn4vzI55ulMqQSvXW9D7iiK0zmf5pt1FT0p_nL4130_provenance.