Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion> ?p ?o ?g. }
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- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion type Assertion NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_head.
- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion description "[No obvious departure was observed between the patients harboring point mutations and large deletions at the 18q21 locus, further supporting TCF4 haploinsufficiency as the molecular mechanism underling PHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_provenance.
- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion evidence source_evidence_literature NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_provenance.
- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion SIO_000772 18781613 NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_provenance.
- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion wasDerivedFrom befree-20140225 NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_provenance.
- NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_assertion wasGeneratedBy ECO_0000203 NP592513.RAh5ankdU4zlMA76Vy-hBMPk4wobMqSR1Ds1311m0Q7_0130_provenance.