Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion type Assertion NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_head.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_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." NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_provenance.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion evidence source_evidence_literature NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_provenance.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion SIO_000772 12812307 NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_provenance.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion wasDerivedFrom befree-20150227 NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_provenance.
- NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_assertion wasGeneratedBy ECO_0000203 NP960075.RAaP-MDVCBKDps83gHd90KspglCN-W1Jt3uDpA0Wra5U0130_provenance.