Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion> ?p ?o ?g. }
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- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion type Assertion NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_head.
- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion wasGeneratedBy ECO_0000203 NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_provenance.
- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion wasDerivedFrom lhgdn-20090331 NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_provenance.
- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion SIO_000772 17704776 NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_provenance.
- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion evidence source_evidence_literature NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_provenance.
- NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_assertion description "[Studies show that the clinical features of the reported disorder resemble those of neurofibromatosis type 1 provide the first report of mutations of SPRED1 (SPROUTY)/SPRED family of genes) in human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151039.RAxe7uWemppywZooMH3K4fcKA_ErM_oN92Ss7sMBZ-vuw130_provenance.