Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion> ?p ?o ?g. }
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- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion type Assertion NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_head.
- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion wasGeneratedBy ECO_0000203 NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_provenance.
- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion wasDerivedFrom lhgdn-20090331 NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_provenance.
- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion SIO_000772 11857550 NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_provenance.
- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion evidence source_evidence_literature NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_provenance.
- NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_assertion description "[May be a modifier of a gene associated with Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193366.RAEMLC_7Jw7ZIr3Vhdi5zyOQM89NAnqrgyR_gdVVhI-2c130_provenance.